rs57758262

Orientation

minus

Stabilized

minus

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

Make rs57758262(A;A)

Make rs57758262(A;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

41571505

Gene

KRT9

is a	snp
is	mentioned by
dbSNP	rs57758262
dbSNP (classic)	rs57758262
ClinGen	rs57758262
ebi	rs57758262
HLI	rs57758262
Exac	rs57758262
Gnomad	rs57758262
Varsome	rs57758262
LitVar	rs57758262
Map	rs57758262
PheGenI	rs57758262
Biobank	rs57758262
1000 genomes	rs57758262
hgdp	rs57758262
ensembl	rs57758262
geneview	rs57758262
scholar	rs57758262
google	rs57758262
pharmgkb	rs57758262
gwascentral	rs57758262
openSNP	rs57758262
23andMe	rs57758262
SNPshot	rs57758262
SNPdbe	rs57758262
MSV3d	rs57758262
GWAS Ctlg	rs57758262

Max Magnitude

0

OMIM	607606
Desc
Variant	0005
Related	also

ClinVar
Risk	rs57758262(A;A) rs57758262(C;C)
Alt	rs57758262(A;A) rs57758262(C;C)
Reference	Rs57758262(G;G)
Significance	Pathogenic
Disease	not provided Epidermolytic palmoplantar keratoderma
Variation	info
Gene	KRT9
CLNDBN	not provided Epidermolytic palmoplantar keratoderma
Reversed	1
HGVS	NC_000017.10:g.39727757C>G; NC_000017.10:g.39727757C>T
CLNSRC	UniProtKB (protein) OMIM Allelic Variant
CLNACC	RCV000056467.1, RCV000003137.2, RCV000056466.1,