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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FIGLA
Indel
(3 prime UTR variant)
Premature ovarian failure
GUncertain significance
CHD7
(G522V)
Single nucleotide variant
(missense variant)
CHARGE association
+5 more
GBenign/Likely benign
TG
(Q870H)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
CYP19A1, MIR4713HG
+1 more
(H128R)
Single nucleotide variant
(missense variant)
Premature ovarian failure
+1 more
GConflicting classifications of pathogenicity
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