List of variants in gene KRT9 reported as likely benign for diffuse palmoplantar keratoderma

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000226.4(KRT9):c.1587T>C (p.Gly529=)	rs146001104	0.01330
NM_000226.4(KRT9):c.1045-9G>A	rs144984735	0.00511
NM_000226.4(KRT9):c.1395-13C>T	rs187834511	0.00480
NM_000226.4(KRT9):c.855G>T (p.Leu285=)	rs115349045	0.00468
NM_000226.4(KRT9):c.351T>C (p.Gly117=)	rs115965791	0.00458
NM_000226.4(KRT9):c.510G>A (p.Lys170=)	rs116096066	0.00382
NM_000226.4(KRT9):c.1170+8G>T	rs150892974	0.00360
NM_000226.4(KRT9):c.245G>A (p.Ser82Asn)	rs148867398	0.00227
NM_000226.4(KRT9):c.948C>T (p.Gly316=)	rs111424754	0.00116
NM_000226.4(KRT9):c.1800C>T (p.Tyr600=)	rs148193621	0.00062
NM_000226.4(KRT9):c.1216T>C (p.Cys406Arg)	rs77688767	0.00043
NM_000226.4(KRT9):c.-57T>C	rs143343698	0.00038
NM_000226.4(KRT9):c.540C>A (p.Asp180Glu)	rs114438618	0.00029
NM_000226.4(KRT9):c.222C>T (p.Gly74=)	rs114665757	0.00026
NM_000226.4(KRT9):c.437G>A (p.Gly146Asp)	rs115534630	0.00006
NM_000226.4(KRT9):c.72C>T (p.Ser24=)	rs369925340	0.00005
NM_000226.4(KRT9):c.1509A>G (p.Gly503=)	rs527491908	0.00001

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