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rs763872353

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs763872353(C;C)
Make rs763872353(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47408483
GeneMSH2
is asnp
is mentioned by
dbSNPrs763872353
ebirs763872353
HLIrs763872353
Exacrs763872353
Varsomers763872353
Maprs763872353
PheGenIrs763872353
hapmaprs763872353
1000 genomesrs763872353
hgdprs763872353
ensemblrs763872353
gopubmedrs763872353
geneviewrs763872353
scholarrs763872353
googlers763872353
pharmgkbrs763872353
gwascentralrs763872353
openSNPrs763872353
23andMers763872353
23andMe allrs763872353
SNP Nexus

SNPshotrs763872353
SNPdbers763872353
MSV3drs763872353
GWAS Ctlgrs763872353
Max Magnitude0
ClinVar
Risk rs763872353(C;C)
Alt rs763872353(C;C)
Reference rs763872353(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47635622T>A
CLNSRC
CLNACC RCV000235827.1,