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rs786204321

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204321(C;T)
Make rs786204321(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47475249
GeneMSH2
is asnp
is mentioned by
dbSNPrs786204321
ebirs786204321
HLIrs786204321
Exacrs786204321
Varsomers786204321
Maprs786204321
PheGenIrs786204321
hapmaprs786204321
1000 genomesrs786204321
hgdprs786204321
ensemblrs786204321
gopubmedrs786204321
geneviewrs786204321
scholarrs786204321
googlers786204321
pharmgkbrs786204321
gwascentralrs786204321
openSNPrs786204321
23andMers786204321
23andMe allrs786204321
SNP Nexus

SNPshotrs786204321
SNPdbers786204321
MSV3drs786204321
GWAS Ctlgrs786204321
Max Magnitude0
ClinVar
Risk rs786204321(T;T)
Alt rs786204321(T;T)
Reference rs786204321(C;C)
Significance Pathogenic
Disease Lynch syndrome I
Variation info
Gene MSH2
CLNDBN Lynch syndrome I
Reversed 0
HGVS NC_000002.11:g.47702388C>T
CLNSRC
CLNACC RCV000168729.1,