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Items: 64

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ROR2
Single nucleotide variant
(3 prime UTR variant)
Brachydactyly type B1
+3 more
GBenign
ROR2
(D935E)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
ROR2
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign
ROR2
(D895G)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
ROR2
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
ROR2
(S861L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ROR2
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
ROR2
(Y830C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ROR2
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign/Likely benign
ROR2
(V821I)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
ROR2
(V819I)
Single nucleotide variant
(missense variant)
not specified
+4 more
GBenign
ROR2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
ROR2
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
ROR2
(P799S)
Single nucleotide variant
(missense variant)
ROR2-related condition
+3 more
GConflicting classifications of pathogenicity
ROR2
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
ROR2
(S762L)
Single nucleotide variant
(missense variant)
Brachydactyly, type B1Robinow syndrome, autosomal recessive
+3 more
GConflicting classifications of pathogenicity
ROR2
(R747Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
ROR2
(A719T)
Single nucleotide variant
(missense variant)
Brachydactyly type B1
+2 more
GUncertain significance
ROR2
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign
ROR2
Duplication
(nonsense)
not provided
GPathogenic
ROR2
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign
ROR2
(G695R)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign
ROR2
(C694R)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
ROR2
(I656V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ROR2
(K647R)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
ROR2
(V629M)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
ROR2
(A586T)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
ROR2
(D579G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ROR2
(D579V)
Single nucleotide variant
(missense variant)
Autosomal recessive Robinow syndrome
+3 more
GConflicting classifications of pathogenicity
ROR2
(H571R)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
ROR2
Single nucleotide variant
(synonymous variant)
not provided
+4 more
GBenign
ROR2
(G559S)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
ROR2
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
ROR2
(S557L)
Single nucleotide variant
(missense variant)
Brachydactyly type B1
+3 more
GConflicting classifications of pathogenicity
ROR2
(R530Q)
Single nucleotide variant
(missense variant)
not provided
+3 more
GBenign/Likely benign
ROR2
(R528Q)
Single nucleotide variant
(missense variant)
Brachydactyly type B1
+3 more
GConflicting classifications of pathogenicity
ROR2
(R522Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
ROR2
(P497L)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
ROR2
(R483Q)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
ROR2
(S447A)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GUncertain significance
ROR2
(S406L)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ROR2
(S401L)
Single nucleotide variant
(missense variant +1 more)
not provided
GConflicting classifications of pathogenicity
ROR2
(R385C)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ROR2
(S352G)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
ROR2
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
ROR2
Single nucleotide variant
(intron variant)
Brachydactyly type B1
+3 more
GBenign/Likely benign
ROR2
(M291V)
Single nucleotide variant
(missense variant)
Autosomal recessive Robinow syndrome
+2 more
GUncertain significance
ROR2
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
ROR2
(I270V)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
ROR2
(T245A)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign
ROR2
(R244W)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
ROR2
Single nucleotide variant
(synonymous variant)
Brachydactyly type B1
+2 more
GUncertain significance
ROR2
(T190A)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
ROR2
(T127M)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
ROR2
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign/Likely benign
ROR2
(A100T)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
ROR2
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
ROR2
(T78R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ROR2
(T78M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ROR2
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
ROR2
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GConflicting classifications of pathogenicity
ROR2
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
ROR2
(L13V)
Single nucleotide variant
(missense variant)
ROR2-related condition
+3 more
GUncertain significance
ROR2
(R3W)
Single nucleotide variant
(missense variant)
not provided
+3 more
GBenign/Likely benign
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