rs59151464

Orientation

minus

Stabilized

minus

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

Make rs59151464(C;T)

Make rs59151464(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

12

Position

52679790

Gene

KRT1

is a	snp
is	mentioned by
dbSNP	rs59151464
dbSNP (classic)	rs59151464
ClinGen	rs59151464
ebi	rs59151464
HLI	rs59151464
Exac	rs59151464
Gnomad	rs59151464
Varsome	rs59151464
LitVar	rs59151464
Map	rs59151464
PheGenI	rs59151464
Biobank	rs59151464
1000 genomes	rs59151464
hgdp	rs59151464
ensembl	rs59151464
geneview	rs59151464
scholar	rs59151464
google	rs59151464
pharmgkb	rs59151464
gwascentral	rs59151464
openSNP	rs59151464
23andMe	rs59151464
SNPshot	rs59151464
SNPdbe	rs59151464
MSV3d	rs59151464
GWAS Ctlg	rs59151464

Max Magnitude

0

ClinVar
Risk	rs59151464(T;T)
Alt	rs59151464(T;T)
Reference	Rs59151464(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KRT1
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.53073574G>A
CLNSRC
CLNACC	RCV000057089.2,