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rs137853010

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853010(C;T)
Make rs137853010(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position28725028
GeneCHEK2
is asnp
is mentioned by
dbSNPrs137853010
ebirs137853010
HLIrs137853010
Exacrs137853010
Varsomers137853010
Maprs137853010
PheGenIrs137853010
hapmaprs137853010
1000 genomesrs137853010
hgdprs137853010
ensemblrs137853010
gopubmedrs137853010
geneviewrs137853010
scholarrs137853010
googlers137853010
pharmgkbrs137853010
gwascentralrs137853010
openSNPrs137853010
23andMers137853010
23andMe allrs137853010
SNP Nexus

SNPshotrs137853010
SNPdbers137853010
MSV3drs137853010
GWAS Ctlgrs137853010
Max Magnitude0
OMIM604373
Desc
Variant0008
Relatedalso
ClinVar
Risk rs137853010(G,T;G,T)
Alt rs137853010(G,T;G,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
CLNACC RCV000005945.5, RCV000164479.1, RCV000196466.2, RCV000216866.1, RCV000160455.1,