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rs121908698

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908698(G;T)
Make rs121908698(T;T)
ReferenceGRCh38 38.1/142
Chromosome22
Position28725242
GeneCHEK2
is asnp
is mentioned by
dbSNPrs121908698
ebirs121908698
HLIrs121908698
Exacrs121908698
Varsomers121908698
Maprs121908698
PheGenIrs121908698
hapmaprs121908698
1000 genomesrs121908698
hgdprs121908698
ensemblrs121908698
gopubmedrs121908698
geneviewrs121908698
scholarrs121908698
googlers121908698
pharmgkbrs121908698
gwascentralrs121908698
openSNPrs121908698
23andMers121908698
23andMe allrs121908698
SNP Nexus

SNPshotrs121908698
SNPdbers121908698
MSV3drs121908698
GWAS Ctlgrs121908698
Max Magnitude0
ClinVar
Risk rs121908698(A,T;A,T)
Alt rs121908698(A,T;A,T)
Reference rs121908698(G;G)
Significance Pathogenic
Disease not provided Familial cancer of breast Hereditary cancer-predisposing syndrome Breast and colorectal cancer
Variation info
Gene CHEK2
CLNDBN not provided Familial cancer of breast Hereditary cancer-predisposing syndrome Breast and colorectal cancer, susceptibility to
Reversed 1
HGVS NC_000022.10:g.29121230C>A; NC_000022.10:g.29121230C>T
CLNSRC ClinVar Ambry Genetics GeneDx
CLNACC RCV000114770.3, RCV000199852.1, RCV000116017.5, RCV000196718.3, RCV000210090.1, RCV000212418.1,