List of variants in gene KRTAP9-3 reported as likely benign by Ambry Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_031962.3(KRTAP9-3):c.329G>C (p.Ser110Thr)	rs778087613	0.00012
NM_031962.3(KRTAP9-3):c.143A>G (p.His48Arg)	rs369726385	0.00008
NM_031962.3(KRTAP9-3):c.11G>C (p.Cys4Ser)
NM_031962.3(KRTAP9-3):c.371A>G (p.Asn124Ser)	rs767184540
NM_031962.3(KRTAP9-3):c.57G>C (p.Trp19Cys)	rs369722249

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