ClinVar Miner

List of variants in gene SDCCAG8 studied for perceptual disorders

Included ClinVar conditions (765):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_006642.5(SDCCAG8):c.778C>G (p.Leu260Val) rs201869920 0.00046
NM_006642.5(SDCCAG8):c.1817_1818dup (p.Ala607Ter)
NM_006642.5(SDCCAG8):c.41T>C (p.Leu14Pro)
NM_006642.5(SDCCAG8):c.89A>G (p.His30Arg)

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