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rs876658834

From SNPedia

Orientationplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs876658834(-;-)
Make rs876658834(-;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47463106
GeneMSH2
is asnp
is mentioned by
dbSNPrs876658834
ebirs876658834
HLIrs876658834
Exacrs876658834
Varsomers876658834
Maprs876658834
PheGenIrs876658834
hapmaprs876658834
1000 genomesrs876658834
hgdprs876658834
ensemblrs876658834
gopubmedrs876658834
geneviewrs876658834
scholarrs876658834
googlers876658834
pharmgkbrs876658834
gwascentralrs876658834
openSNPrs876658834
23andMers876658834
23andMe allrs876658834
SNP Nexus

SNPshotrs876658834
SNPdbers876658834
MSV3drs876658834
GWAS Ctlgrs876658834
Max Magnitude0
ClinVar
Risk rs876658834(;)
Alt rs876658834(;)
Reference rs876658834(TT;TT)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.47690245_47690246delTT
CLNSRC
CLNACC RCV000220873.1,