RS769120800 ATP6V0A2

Health Risk Chr 12:123737209
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Associated Conditions
ALG9 congenital disorder of glycosylation
Inborn genetic diseases
Cutis laxa with osteodystrophy
Wrinkly skin syndrome
ALG9 congenital disorder of glycosylation
Inborn genetic diseases
Cutis laxa with osteodystrophy
Wrinkly skin syndrome
Other Variants in ATP6V0A2
rs80356758 rs80356750 rs80356755 rs80356756 rs367543007 rs80356751 rs80356753 rs1566294545 rs181112338 rs374480381
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