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Items: 1 to 100 of 142

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LRRK2
(E10K)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
Single nucleotide variant
(no sequence alteration)
not specified
+1 more
GBenign
LRRK2
(S52F)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+2 more
GBenign/Likely benign
LRRK2
(L119P)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LRRK2
Single nucleotide variant
(no sequence alteration)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
LRRK2
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
LRRK2
(A211V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LRRK2
(C228S)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(S231P)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(N238I)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
Single nucleotide variant
(no sequence alteration)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(L286V)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
LRRK2
Single nucleotide variant
(no sequence alteration)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
Single nucleotide variant
(synonymous variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+2 more
GBenign/Likely benign
LRRK2
(E334K)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
LRRK2
(N363S)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(V366M)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(L378F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LRRK2
(A419V)
Single nucleotide variant
(missense variant)
LRRK2-related condition
+2 more
GBenign/Likely benign
LRRK2
(V430I)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
Single nucleotide variant
(no sequence alteration)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
LRRK2
(R506Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
LRRK2
(R521G)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
LRRK2
(K544E)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(N551K)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign
LRRK2
Single nucleotide variant
(no sequence alteration)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(I610T)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(K616R)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(S663P)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+2 more
GBenign/Likely benign
LRRK2
(M712V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LRRK2
(A716V)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(I723V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign
LRRK2
(P755L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
LRRK2
(R772*)
Single nucleotide variant
(nonsense)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(R793M)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LRRK2
(I810V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LRRK2
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+1 more
GLikely benign
LRRK2
(K871E)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(Q923H)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LRRK2
(Q930R)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(D944Y)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
LRRK2
(S973N)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(I1006M)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
Single nucleotide variant
(no sequence alteration)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(L1063F)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
LRRK2
(R1067Q)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(S1096C)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(Q1111H)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
LRRK2
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+4 more
GBenign/Likely benign
LRRK2
(I1122V)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GPathogenic
LRRK2
(A1151T)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(L1165P)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(I1192V)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(H1216R)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(S1228I)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(S1228T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LRRK2
(P1262A)
Single nucleotide variant
(missense variant)
LRRK2-related condition
+2 more
GBenign/Likely benign
LRRK2
(R1320S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
LRRK2
(R1325Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LRRK2
(I1371V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
LRRK2
(D1375E)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(R1398H)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
LRRK2
(T1410M)
Single nucleotide variant
(missense variant)
LRRK2-related condition
+2 more
GBenign/Likely benign
LRRK2
(D1420N)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
LRRK2
Single nucleotide variant
(synonymous variant)
LRRK2-related condition
+1 more
GLikely benign
LRRK2
(N1437H)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(I1438M)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(R1441C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
LRRK2
(R1441G)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
+1 more
GPathogenic
LRRK2
(R1441H)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GPathogenic
LRRK2
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+1 more
GLikely benign
LRRK2
(A1442P)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(P1446L)
Single nucleotide variant
(missense variant)
LRRK2-related condition
+1 more
GLikely benign
LRRK2
(V1450I)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(H1453R)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(D1455fs)
Deletion
(frameshift variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(K1468E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LRRK2
(A1481T)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(R1483Q)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GUncertain significance
LRRK2
(R1514Q)
Single nucleotide variant
(missense variant)
LRRK2-related condition
+2 more
GBenign/Likely benign
LRRK2
(P1542S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
LRRK2
(L1556I)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(V1598E)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
(V1613A)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
Gnot provided
LRRK2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
LRRK2
(R1628P)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
LRRK2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
LRRK2
(M1646T)
Single nucleotide variant
(missense variant)
LRRK2-related condition
+2 more
GBenign/Likely benign
LRRK2
(S1647T)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
+1 more
GBenign
LRRK2
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+1 more
GBenign/Likely benign
LRRK2
(Y1699C)
Single nucleotide variant
(missense variant)
Autosomal dominant Parkinson disease 8
GPathogenic
LRRK2
Single nucleotide variant
(synonymous variant)
LRRK2-related condition
+3 more
GBenign/Likely benign
LRRK2
(R1725*)
Single nucleotide variant
(nonsense)
Autosomal dominant Parkinson disease 8
Gnot provided
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