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rs878854926

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854926(A;A)
Make rs878854926(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28703567
GeneCHEK2
is asnp
is mentioned by
dbSNPrs878854926
ebirs878854926
HLIrs878854926
Exacrs878854926
Varsomers878854926
Maprs878854926
PheGenIrs878854926
hapmaprs878854926
1000 genomesrs878854926
hgdprs878854926
ensemblrs878854926
gopubmedrs878854926
geneviewrs878854926
scholarrs878854926
googlers878854926
pharmgkbrs878854926
gwascentralrs878854926
openSNPrs878854926
23andMers878854926
23andMe allrs878854926
SNP Nexus

SNPshotrs878854926
SNPdbers878854926
MSV3drs878854926
GWAS Ctlgrs878854926
Max Magnitude0
ClinVar
Risk rs878854926(A;A)
Alt rs878854926(A;A)
Reference rs878854926(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000022.10:g.29099555C>T
CLNSRC
CLNACC RCV000227592.1,