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rs786204257

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204257(-;-)
Make rs786204257(-;T)
Make rs786204257(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47408450
GeneMSH2
is asnp
is mentioned by
dbSNPrs786204257
ebirs786204257
HLIrs786204257
Exacrs786204257
Varsomers786204257
Maprs786204257
PheGenIrs786204257
hapmaprs786204257
1000 genomesrs786204257
hgdprs786204257
ensemblrs786204257
gopubmedrs786204257
geneviewrs786204257
scholarrs786204257
googlers786204257
pharmgkbrs786204257
gwascentralrs786204257
openSNPrs786204257
23andMers786204257
23andMe allrs786204257
SNP Nexus

SNPshotrs786204257
SNPdbers786204257
MSV3drs786204257
GWAS Ctlgrs786204257
Max Magnitude0
ClinVar
Risk rs786204257(T;T)
Alt rs786204257(T;T)
Reference rs786204257(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47635589dupT
CLNSRC
CLNACC RCV000168462.1,