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rs876658302

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658302(-;-)
Make rs876658302(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28695772
GeneCHEK2
is asnp
is mentioned by
dbSNPrs876658302
ebirs876658302
HLIrs876658302
Exacrs876658302
Varsomers876658302
Maprs876658302
PheGenIrs876658302
hapmaprs876658302
1000 genomesrs876658302
hgdprs876658302
ensemblrs876658302
gopubmedrs876658302
geneviewrs876658302
scholarrs876658302
googlers876658302
pharmgkbrs876658302
gwascentralrs876658302
openSNPrs876658302
23andMers876658302
23andMe allrs876658302
SNP Nexus

SNPshotrs876658302
SNPdbers876658302
MSV3drs876658302
GWAS Ctlgrs876658302
Max Magnitude0
ClinVar
Risk rs876658302(;)
Alt rs876658302(;)
Reference rs876658302(T;T)
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.29091760delA
CLNSRC
CLNACC RCV000223384.1,