Have questions? Visit https://www.reddit.com/r/SNPedia

rs137853011

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs137853011(C;T)
Make rs137853011(T;T)
ReferenceGRCh38 38.1/142
Chromosome22
Position28695219
GeneCHEK2
is asnp
is mentioned by
dbSNPrs137853011
ebirs137853011
HLIrs137853011
Exacrs137853011
Varsomers137853011
Maprs137853011
PheGenIrs137853011
hapmaprs137853011
1000 genomesrs137853011
hgdprs137853011
ensemblrs137853011
gopubmedrs137853011
geneviewrs137853011
scholarrs137853011
googlers137853011
pharmgkbrs137853011
gwascentralrs137853011
openSNPrs137853011
23andMers137853011
23andMe allrs137853011
SNP Nexus

SNPshotrs137853011
SNPdbers137853011
MSV3drs137853011
GWAS Ctlgrs137853011
Max Magnitude0
OMIM604373
Desc
Variant0014
Relatedalso
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
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
Reversed 1
HGVS NC_000022.10:g.29091207G>A
CLNSRC Inc. OMIM Allelic Variant
CLNACC RCV000005953.2, RCV000115994.6, RCV000197718.3, RCV000210180.1, RCV000212459.2,