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rs137853009

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853009(A;A)
Make rs137853009(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position28725030
GeneCHEK2
is asnp
is mentioned by
dbSNPrs137853009
ebirs137853009
HLIrs137853009
Exacrs137853009
Varsomers137853009
Maprs137853009
PheGenIrs137853009
hapmaprs137853009
1000 genomesrs137853009
hgdprs137853009
ensemblrs137853009
gopubmedrs137853009
geneviewrs137853009
scholarrs137853009
googlers137853009
pharmgkbrs137853009
gwascentralrs137853009
openSNPrs137853009
23andMers137853009
23andMe allrs137853009
SNP Nexus

SNPshotrs137853009
SNPdbers137853009
MSV3drs137853009
GWAS Ctlgrs137853009
GMAF0.0004591
Max Magnitude0
OMIM604373
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137853009(A;A)
Alt rs137853009(A;A)
Reference rs137853009(G;G)
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.29121018C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005944.5, RCV000116025.5, RCV000206384.1, RCV000212427.1,