rs60090257

Orientation

minus

Stabilized

minus

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

Make rs60090257(A;A)

Make rs60090257(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

41583772

Gene

KRT14

is a	snp
is	mentioned by
dbSNP	rs60090257
dbSNP (classic)	rs60090257
ClinGen	rs60090257
ebi	rs60090257
HLI	rs60090257
Exac	rs60090257
Gnomad	rs60090257
Varsome	rs60090257
LitVar	rs60090257
Map	rs60090257
PheGenI	rs60090257
Biobank	rs60090257
1000 genomes	rs60090257
hgdp	rs60090257
ensembl	rs60090257
geneview	rs60090257
scholar	rs60090257
google	rs60090257
pharmgkb	rs60090257
gwascentral	rs60090257
openSNP	rs60090257
23andMe	rs60090257
SNPshot	rs60090257
SNPdbe	rs60090257
MSV3d	rs60090257
GWAS Ctlg	rs60090257

Max Magnitude

0

ClinVar
Risk	rs60090257(A;A)
Alt	rs60090257(A;A)
Reference	Rs60090257(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KRT14
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.39740024C>T
CLNSRC
CLNACC	RCV000056757.2,