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rs876660533

From SNPedia

Orientationplus
Geno Mag Summary
(GGAGCAAAGAA;GGAGCAAAGAA) 0 common in clinvar
Make rs876660533(CAC;CAC)
Make rs876660533(CAC;GGAGCAAAGAA)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47408400
GeneMSH2
is asnp
is mentioned by
dbSNPrs876660533
ebirs876660533
HLIrs876660533
Exacrs876660533
Varsomers876660533
Maprs876660533
PheGenIrs876660533
hapmaprs876660533
1000 genomesrs876660533
hgdprs876660533
ensemblrs876660533
gopubmedrs876660533
geneviewrs876660533
scholarrs876660533
googlers876660533
pharmgkbrs876660533
gwascentralrs876660533
openSNPrs876660533
23andMers876660533
23andMe allrs876660533
SNP Nexus

SNPshotrs876660533
SNPdbers876660533
MSV3drs876660533
GWAS Ctlgrs876660533
Max Magnitude0
ClinVar
Risk rs876660533(CAC;CAC)
Alt rs876660533(CAC;CAC)
Reference rs876660533(GGAGCAAAGAA;GGAGCAAAGAA)
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.47635539_47635549delGGAGCAAAGAAinsCAC
CLNSRC
CLNACC RCV000216646.1,