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rs876660480

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660480(-;-)
Make rs876660480(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47403351
GeneMSH2
is asnp
is mentioned by
dbSNPrs876660480
ebirs876660480
HLIrs876660480
Exacrs876660480
Varsomers876660480
Maprs876660480
PheGenIrs876660480
hapmaprs876660480
1000 genomesrs876660480
hgdprs876660480
ensemblrs876660480
gopubmedrs876660480
geneviewrs876660480
scholarrs876660480
googlers876660480
pharmgkbrs876660480
gwascentralrs876660480
openSNPrs876660480
23andMers876660480
23andMe allrs876660480
SNP Nexus

SNPshotrs876660480
SNPdbers876660480
MSV3drs876660480
GWAS Ctlgrs876660480
Max Magnitude0
ClinVar
Risk rs876660480(;)
Alt rs876660480(;)
Reference rs876660480(G;G)
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.47630490delG
CLNSRC
CLNACC RCV000213902.1,