ClinVar Miner

List of variants in gene combination ATP6V0A2, LOC130009117 reported as uncertain significance for Cutis laxa with osteodystrophy; Wrinkly skin syndrome

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Gene type: Distinguish antisense genes from sense genes
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_012463.4(ATP6V0A2):c.28A>G (p.Met10Val)	rs758214692	0.00009
NM_012463.4(ATP6V0A2):c.26C>T (p.Thr9Ile)	rs752689489	0.00004

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