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Items: 30

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADGRG1
(S5L)
Single nucleotide variant
(missense variant +2 more)
Bilateral frontoparietal polymicrogyria
+1 more
GConflicting classifications of pathogenicity
ADGRG1
Single nucleotide variant
(synonymous variant +2 more)
not provided
GConflicting classifications of pathogenicity
ADGRG1
(R33C +1 more)
Single nucleotide variant
(missense variant +2 more)
Bilateral frontoparietal polymicrogyria
+2 more
GConflicting classifications of pathogenicity
ADGRG1
Single nucleotide variant
(synonymous variant +2 more)
not specified
+2 more
GBenign
ADGRG1
Single nucleotide variant
(synonymous variant +2 more)
not specified
+3 more
GBenign/Likely benign
ADGRG1
(T66I +1 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
ADGRG1
(A69S +1 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
ADGRG1
Single nucleotide variant
(synonymous variant +2 more)
ADGRG1-related condition
+1 more
GConflicting classifications of pathogenicity
ADGRG1
(R108H +2 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
ADGRG1
(Q125E +2 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
+1 more
GUncertain significance
ADGRG1
(Q131H +2 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
ADGRG1
(S163R +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
+2 more
GConflicting classifications of pathogenicity
ADGRG1
(S214W +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADGRG1
(S281R +4 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
ADGRG1
(G282R +4 more)
Single nucleotide variant
(missense variant)
ADGRG1-related condition
+4 more
GBenign/Likely benign
ADGRG1
Single nucleotide variant
(intron variant)
not specified
+3 more
GBenign/Likely benign
ADGRG1
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
ADGRG1
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
ADGRG1
(V398A +5 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
ADGRG1
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign/Likely benign
ADGRG1
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
ADGRG1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
ADGRG1
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
ADGRG1
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
ADGRG1
(R598W +7 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADGRG1
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
ADGRG1
(L625F +7 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADGRG1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
ADGRG1
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GConflicting classifications of pathogenicity
ADGRG1
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
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