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rs876660801

From SNPedia

Orientationminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs876660801(-;-)
Make rs876660801(-;GT)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28695125
GeneCHEK2
is asnp
is mentioned by
dbSNPrs876660801
ebirs876660801
HLIrs876660801
Exacrs876660801
Varsomers876660801
Maprs876660801
PheGenIrs876660801
hapmaprs876660801
1000 genomesrs876660801
hgdprs876660801
ensemblrs876660801
gopubmedrs876660801
geneviewrs876660801
scholarrs876660801
googlers876660801
pharmgkbrs876660801
gwascentralrs876660801
openSNPrs876660801
23andMers876660801
23andMe allrs876660801
SNP Nexus

SNPshotrs876660801
SNPdbers876660801
MSV3drs876660801
GWAS Ctlgrs876660801
Max Magnitude0
ClinVar
Risk rs876660801(;)
Alt rs876660801(;)
Reference rs876660801(GT;GT)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CHEK2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000022.10:g.29091113_29091114delAC
CLNSRC
CLNACC RCV000220512.1,