rs61157095

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs61157095(C;C)

Make rs61157095(C;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

41571490

Gene

KRT9

is a	snp
is	mentioned by
dbSNP	rs61157095
dbSNP (classic)	rs61157095
ClinGen	rs61157095
ebi	rs61157095
HLI	rs61157095
Exac	rs61157095
Gnomad	rs61157095
Varsome	rs61157095
LitVar	rs61157095
Map	rs61157095
PheGenI	rs61157095
Biobank	rs61157095
1000 genomes	rs61157095
hgdp	rs61157095
ensembl	rs61157095
geneview	rs61157095
scholar	rs61157095
google	rs61157095
pharmgkb	rs61157095
gwascentral	rs61157095
openSNP	rs61157095
23andMe	rs61157095
SNPshot	rs61157095
SNPdbe	rs61157095
MSV3d	rs61157095
GWAS Ctlg	rs61157095

Max Magnitude

0

OMIM	607606
Desc
Variant	0008
Related	also

ClinVar
Risk	rs61157095(C;C)
Alt	rs61157095(C;C)
Reference	Rs61157095(T;T)
Significance	Pathogenic
Disease	Epidermolytic palmoplantar keratoderma not provided
Variation	info
Gene	KRT9
CLNDBN	Epidermolytic palmoplantar keratoderma not provided
Reversed	1
HGVS	NC_000017.10:g.39727742A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000003140.2, RCV000056469.1,