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rs121908707

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908707(C;C)
Make rs121908707(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position28695709
GeneCHEK2
is asnp
is mentioned by
dbSNPrs121908707
dbSNP (old)rs121908707
ClinGenrs121908707
ebirs121908707
HLIrs121908707
Exacrs121908707
Gnomadrs121908707
Varsomers121908707
Maprs121908707
PheGenIrs121908707
Biobankrs121908707
1000 genomesrs121908707
hgdprs121908707
ensemblrs121908707
gopubmedrs121908707
geneviewrs121908707
scholarrs121908707
googlers121908707
pharmgkbrs121908707
gwascentralrs121908707
openSNPrs121908707
23andMers121908707
23andMe allrs121908707
SNPshotrs121908707
SNPdbers121908707
MSV3drs121908707
GWAS Ctlgrs121908707
Max Magnitude0
ClinVar
Risk rs121908707(C;C) rs121908707(T;T)
Alt rs121908707(C;C) rs121908707(T;T)
Reference Rs121908707(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast not provided
Variation info
Gene CHEK2
CLNDBN Familial cancer of breast not provided
Reversed 1
HGVS NC_000022.10:g.29091697C>A; NC_000022.10:g.29091697C>G
CLNSRC
CLNACC RCV000465281.1, RCV000114767.2,