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rs121908701

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121908701(A;A)
Make rs121908701(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position28725027
GeneCHEK2
is asnp
is mentioned by
dbSNPrs121908701
ebirs121908701
HLIrs121908701
Exacrs121908701
Varsomers121908701
Maprs121908701
PheGenIrs121908701
hapmaprs121908701
1000 genomesrs121908701
hgdprs121908701
ensemblrs121908701
gopubmedrs121908701
geneviewrs121908701
scholarrs121908701
googlers121908701
pharmgkbrs121908701
gwascentralrs121908701
openSNPrs121908701
23andMers121908701
23andMe allrs121908701
SNP Nexus

SNPshotrs121908701
SNPdbers121908701
MSV3drs121908701
GWAS Ctlgrs121908701
Max Magnitude0
OMIM604373
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121908701(A;A)
Alt rs121908701(A;A)
Reference rs121908701(G;G)
Significance Pathogenic
Disease Prostate cancer not provided Hereditary cancer-predisposing syndrome not specified Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN Prostate cancer, somatic not provided Hereditary cancer-predisposing syndrome not specified Familial cancer of breast
Reversed 1
HGVS NC_000022.10:g.29121015C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005946.5, RCV000114761.1, RCV000129670.4, RCV000212428.1, RCV000233960.1,


[PMID 12533788OA-icon.png] Mutations in CHEK2 associated with prostate cancer risk.


[PMID 15095295] Limited relevance of the CHEK2 gene in hereditary breast cancer.