rs60297570

Orientation

minus

Stabilized

minus

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

Make rs60297570(C;T)

Make rs60297570(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

12

Position

52678650

Gene

KRT1

is a	snp
is	mentioned by
dbSNP	rs60297570
dbSNP (classic)	rs60297570
ClinGen	rs60297570
ebi	rs60297570
HLI	rs60297570
Exac	rs60297570
Gnomad	rs60297570
Varsome	rs60297570
LitVar	rs60297570
Map	rs60297570
PheGenI	rs60297570
Biobank	rs60297570
1000 genomes	rs60297570
hgdp	rs60297570
ensembl	rs60297570
geneview	rs60297570
scholar	rs60297570
google	rs60297570
pharmgkb	rs60297570
gwascentral	rs60297570
openSNP	rs60297570
23andMe	rs60297570
SNPshot	rs60297570
SNPdbe	rs60297570
MSV3d	rs60297570
GWAS Ctlg	rs60297570

Max Magnitude

0

ClinVar
Risk	rs60297570(T;T)
Alt	rs60297570(T;T)
Reference	Rs60297570(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KRT1
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.53072434G>A
CLNSRC
CLNACC	RCV000057104.2,