rs58645163

Orientation

minus

Stabilized

minus

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

Make rs58645163(A;A)

Make rs58645163(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

41583346

Gene

KRT14

is a	snp
is	mentioned by
dbSNP	rs58645163
dbSNP (classic)	rs58645163
ClinGen	rs58645163
ebi	rs58645163
HLI	rs58645163
Exac	rs58645163
Gnomad	rs58645163
Varsome	rs58645163
LitVar	rs58645163
Map	rs58645163
PheGenI	rs58645163
Biobank	rs58645163
1000 genomes	rs58645163
hgdp	rs58645163
ensembl	rs58645163
geneview	rs58645163
scholar	rs58645163
google	rs58645163
pharmgkb	rs58645163
gwascentral	rs58645163
openSNP	rs58645163
23andMe	rs58645163
SNPshot	rs58645163
SNPdbe	rs58645163
MSV3d	rs58645163
GWAS Ctlg	rs58645163

Max Magnitude

0

ClinVar
Risk	rs58645163(A;A) rs58645163(C;C)
Alt	rs58645163(A;A) rs58645163(C;C)
Reference	Rs58645163(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KRT14
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.39739598C>G; NC_000017.10:g.39739598C>T
CLNSRC
CLNACC	RCV000056670.1, RCV000487370.1,