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rs876659519

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659519(G;G)
Make rs876659519(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28703519
GeneCHEK2
is asnp
is mentioned by
dbSNPrs876659519
ebirs876659519
HLIrs876659519
Exacrs876659519
Varsomers876659519
Maprs876659519
PheGenIrs876659519
hapmaprs876659519
1000 genomesrs876659519
hgdprs876659519
ensemblrs876659519
gopubmedrs876659519
geneviewrs876659519
scholarrs876659519
googlers876659519
pharmgkbrs876659519
gwascentralrs876659519
openSNPrs876659519
23andMers876659519
23andMe allrs876659519
SNP Nexus

SNPshotrs876659519
SNPdbers876659519
MSV3drs876659519
GWAS Ctlgrs876659519
Max Magnitude0
ClinVar
Risk rs876659519(G;G)
Alt rs876659519(G;G)
Reference rs876659519(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.29099507A>C
CLNSRC
CLNACC RCV000215015.1,