ClinVar Miner

List of variants studied for autosomal dominant nonsyndromic hearing loss 2A by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (1):

Autosomal dominant nonsyndromic hearing loss 2A

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004700.4(KCNQ4):c.665G>A (p.Gly222Asp)	rs752658856	0.00006
NM_004700.4(KCNQ4):c.682G>T (p.Gly228Cys)	rs367890569	0.00003
NM_004700.4(KCNQ4):c.733G>A (p.Gly245Arg)
NM_004700.4(KCNQ4):c.829G>A (p.Gly277Arg)	rs727504459

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