rs137853011

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common on affy axiom data

Make rs137853011(C;T)

Make rs137853011(T;T)

Reference

GRCh38 38.1/142

Chromosome

22

Position

28695219

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs137853011
dbSNP (classic)	rs137853011
ClinGen	rs137853011
ebi	rs137853011
HLI	rs137853011
Exac	rs137853011
Gnomad	rs137853011
Varsome	rs137853011
LitVar	rs137853011
Map	rs137853011
PheGenI	rs137853011
Biobank	rs137853011
1000 genomes	rs137853011
hgdp	rs137853011
ensembl	rs137853011
geneview	rs137853011
scholar	rs137853011
google	rs137853011
pharmgkb	rs137853011
gwascentral	rs137853011
openSNP	rs137853011
23andMe	rs137853011
SNPshot	rs137853011
SNPdbe	rs137853011
MSV3d	rs137853011
GWAS Ctlg	rs137853011

Max Magnitude

0

OMIM	604373
Desc
Variant	0014
Related	also

ClinVar
Risk	rs137853011(T;T)
Alt	rs137853011(T;T)
Reference	Rs137853011(C;C)
Significance	Other
Disease	Breast cancer Hereditary cancer-predisposing syndrome Familial cancer of breast Breast and colorectal cancer not provided Colorectal cancer Neoplasm of breast
Variation	info
Gene	CHEK2
CLNDBN	Breast cancer, susceptibility to Hereditary cancer-predisposing syndrome Familial cancer of breast Breast and colorectal cancer, susceptibility to not provided Colorectal cancer Neoplasm of breast
Reversed	1
HGVS	NC_000022.10:g.29091207G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005953.2, RCV000115994.8, RCV000197718.4, RCV000210180.1, RCV000212459.3, RCV000277703.1, RCV000388223.1,