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rs876660862

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660862(-;-)
Make rs876660862(-;T)
Make rs876660862(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28703536
GeneCHEK2
is asnp
is mentioned by
dbSNPrs876660862
ebirs876660862
HLIrs876660862
Exacrs876660862
Varsomers876660862
Maprs876660862
PheGenIrs876660862
hapmaprs876660862
1000 genomesrs876660862
hgdprs876660862
ensemblrs876660862
gopubmedrs876660862
geneviewrs876660862
scholarrs876660862
googlers876660862
pharmgkbrs876660862
gwascentralrs876660862
openSNPrs876660862
23andMers876660862
23andMe allrs876660862
SNP Nexus

SNPshotrs876660862
SNPdbers876660862
MSV3drs876660862
GWAS Ctlgrs876660862
Max Magnitude0
ClinVar
Risk rs876660862(T;T)
Alt rs876660862(T;T)
Reference rs876660862(;)
Significance 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.29099525dupA
CLNSRC
CLNACC RCV000213838.1,