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rs876659639

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659639(-;-)
Make rs876659639(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28695165
GeneCHEK2
is asnp
is mentioned by
dbSNPrs876659639
ebirs876659639
HLIrs876659639
Exacrs876659639
Varsomers876659639
Maprs876659639
PheGenIrs876659639
hapmaprs876659639
1000 genomesrs876659639
hgdprs876659639
ensemblrs876659639
gopubmedrs876659639
geneviewrs876659639
scholarrs876659639
googlers876659639
pharmgkbrs876659639
gwascentralrs876659639
openSNPrs876659639
23andMers876659639
23andMe allrs876659639
SNP Nexus

SNPshotrs876659639
SNPdbers876659639
MSV3drs876659639
GWAS Ctlgrs876659639
Max Magnitude0
ClinVar
Risk rs876659639(;)
Alt rs876659639(;)
Reference rs876659639(A;A)
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.29091153delT
CLNSRC
CLNACC RCV000219411.1,