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rs878854917

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854917(G;T)
Make rs878854917(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28734514
GeneCHEK2
is asnp
is mentioned by
dbSNPrs878854917
dbSNP (old)rs878854917
ClinGenrs878854917
ebirs878854917
HLIrs878854917
Exacrs878854917
Gnomadrs878854917
Varsomers878854917
Maprs878854917
PheGenIrs878854917
Biobankrs878854917
1000 genomesrs878854917
hgdprs878854917
ensemblrs878854917
gopubmedrs878854917
geneviewrs878854917
scholarrs878854917
googlers878854917
pharmgkbrs878854917
gwascentralrs878854917
openSNPrs878854917
23andMers878854917
23andMe allrs878854917
SNP Nexus

SNPshotrs878854917
SNPdbers878854917
MSV3drs878854917
GWAS Ctlgrs878854917
Max Magnitude0
ClinVar
Risk rs878854917(T;T)
Alt rs878854917(T;T)
Reference Rs878854917(G;G)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000022.10:g.29130502C>A
CLNSRC
CLNACC RCV000228482.1,