rs137853010

Orientation

minus

Stabilized

minus

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

Make rs137853010(C;T)

Make rs137853010(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

28725028

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs137853010
dbSNP (classic)	rs137853010
ClinGen	rs137853010
ebi	rs137853010
HLI	rs137853010
Exac	rs137853010
Gnomad	rs137853010
Varsome	rs137853010
LitVar	rs137853010
Map	rs137853010
PheGenI	rs137853010
Biobank	rs137853010
1000 genomes	rs137853010
hgdp	rs137853010
ensembl	rs137853010
geneview	rs137853010
scholar	rs137853010
google	rs137853010
pharmgkb	rs137853010
gwascentral	rs137853010
openSNP	rs137853010
23andMe	rs137853010
SNPshot	rs137853010
SNPdbe	rs137853010
MSV3d	rs137853010
GWAS Ctlg	rs137853010

Max Magnitude

0

OMIM	604373
Desc
Variant	0008
Related	also

ClinVar
Risk	rs137853010(G;G) rs137853010(T;T)
Alt	rs137853010(G;G) rs137853010(T;T)
Reference	Rs137853010(C;C)
Significance	Pathogenic
Disease	Prostate cancer Hereditary cancer-predisposing syndrome Familial cancer of breast not specified
Variation	info
Gene	CHEK2
CLNDBN	Prostate cancer, somatic Hereditary cancer-predisposing syndrome Familial cancer of breast not specified
Reversed	1
HGVS	NC_000022.10:g.29121016G>A; NC_000022.10:g.29121016G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005945.5, RCV000164479.2, RCV000196466.3, RCV000216866.2, RCV000160455.1,