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rs876659131

From SNPedia

Orientationminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs876659131(-;-)
Make rs876659131(-;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position28703537
GeneCHEK2
is asnp
is mentioned by
dbSNPrs876659131
ebirs876659131
HLIrs876659131
Exacrs876659131
Varsomers876659131
Maprs876659131
PheGenIrs876659131
hapmaprs876659131
1000 genomesrs876659131
hgdprs876659131
ensemblrs876659131
gopubmedrs876659131
geneviewrs876659131
scholarrs876659131
googlers876659131
pharmgkbrs876659131
gwascentralrs876659131
openSNPrs876659131
23andMers876659131
23andMe allrs876659131
SNP Nexus

SNPshotrs876659131
SNPdbers876659131
MSV3drs876659131
GWAS Ctlgrs876659131
Max Magnitude0
ClinVar
Risk rs876659131(;)
Alt rs876659131(;)
Reference rs876659131(TT;TT)
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.29099525_29099526delAA
CLNSRC
CLNACC RCV000219196.1,