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rs878854909

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854909(C;T)
Make rs878854909(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28696924
GeneCHEK2
is asnp
is mentioned by
dbSNPrs878854909
ebirs878854909
HLIrs878854909
Exacrs878854909
Varsomers878854909
Maprs878854909
PheGenIrs878854909
hapmaprs878854909
1000 genomesrs878854909
hgdprs878854909
ensemblrs878854909
gopubmedrs878854909
geneviewrs878854909
scholarrs878854909
googlers878854909
pharmgkbrs878854909
gwascentralrs878854909
openSNPrs878854909
23andMers878854909
23andMe allrs878854909
SNP Nexus

SNPshotrs878854909
SNPdbers878854909
MSV3drs878854909
GWAS Ctlgrs878854909
Max Magnitude0
ClinVar
Risk rs878854909(T;T)
Alt rs878854909(T;T)
Reference rs878854909(C;C)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000022.10:g.29092912G>A
CLNSRC
CLNACC RCV000229454.1,