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rs876661156

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876661156(-;-)
Make rs876661156(-;C)
Make rs876661156(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28734445
GeneCHEK2
is asnp
is mentioned by
dbSNPrs876661156
ebirs876661156
HLIrs876661156
Exacrs876661156
Varsomers876661156
Maprs876661156
PheGenIrs876661156
hapmaprs876661156
1000 genomesrs876661156
hgdprs876661156
ensemblrs876661156
gopubmedrs876661156
geneviewrs876661156
scholarrs876661156
googlers876661156
pharmgkbrs876661156
gwascentralrs876661156
openSNPrs876661156
23andMers876661156
23andMe allrs876661156
SNP Nexus

SNPshotrs876661156
SNPdbers876661156
MSV3drs876661156
GWAS Ctlgrs876661156
Max Magnitude0
ClinVar
Risk rs876661156(C;C)
Alt rs876661156(C;C)
Reference rs876661156(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHEK2
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.29130434dupG
CLNSRC
CLNACC RCV000223018.1,