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rs876659287

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659287(A;A)
Make rs876659287(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28694118
GeneCHEK2
is asnp
is mentioned by
dbSNPrs876659287
ebirs876659287
HLIrs876659287
Exacrs876659287
Varsomers876659287
Maprs876659287
PheGenIrs876659287
hapmaprs876659287
1000 genomesrs876659287
hgdprs876659287
ensemblrs876659287
gopubmedrs876659287
geneviewrs876659287
scholarrs876659287
googlers876659287
pharmgkbrs876659287
gwascentralrs876659287
openSNPrs876659287
23andMers876659287
23andMe allrs876659287
SNP Nexus

SNPshotrs876659287
SNPdbers876659287
MSV3drs876659287
GWAS Ctlgrs876659287
Max Magnitude0
ClinVar
Risk rs876659287(A;A)
Alt rs876659287(A;A)
Reference rs876659287(G;G)
Significance Probable-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.29090106C>T
CLNSRC
CLNACC RCV000217905.1,