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rs876661050

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661050(-;-)
Make rs876661050(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28725315
GeneCHEK2
is asnp
is mentioned by
dbSNPrs876661050
ebirs876661050
HLIrs876661050
Exacrs876661050
Varsomers876661050
Maprs876661050
PheGenIrs876661050
hapmaprs876661050
1000 genomesrs876661050
hgdprs876661050
ensemblrs876661050
gopubmedrs876661050
geneviewrs876661050
scholarrs876661050
googlers876661050
pharmgkbrs876661050
gwascentralrs876661050
openSNPrs876661050
23andMers876661050
23andMe allrs876661050
SNP Nexus

SNPshotrs876661050
SNPdbers876661050
MSV3drs876661050
GWAS Ctlgrs876661050
Max Magnitude0
ClinVar
Risk rs876661050(;)
Alt rs876661050(;)
Reference rs876661050(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHEK2
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.29121303delG
CLNSRC
CLNACC RCV000221519.1,