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rs876659833

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659833(G;T)
Make rs876659833(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28734418
GeneCHEK2
is asnp
is mentioned by
dbSNPrs876659833
ebirs876659833
HLIrs876659833
Exacrs876659833
Varsomers876659833
Maprs876659833
PheGenIrs876659833
hapmaprs876659833
1000 genomesrs876659833
hgdprs876659833
ensemblrs876659833
gopubmedrs876659833
geneviewrs876659833
scholarrs876659833
googlers876659833
pharmgkbrs876659833
gwascentralrs876659833
openSNPrs876659833
23andMers876659833
23andMe allrs876659833
SNP Nexus

SNPshotrs876659833
SNPdbers876659833
MSV3drs876659833
GWAS Ctlgrs876659833
Max Magnitude0
ClinVar
Risk rs876659833(T;T)
Alt rs876659833(T;T)
Reference rs876659833(G;G)
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.29130406C>A
CLNSRC
CLNACC RCV000218820.1,