Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779193

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779193(G;T)
Make rs587779193(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47414419
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779193
ebirs587779193
HLIrs587779193
Exacrs587779193
Varsomers587779193
Maprs587779193
PheGenIrs587779193
hapmaprs587779193
1000 genomesrs587779193
hgdprs587779193
ensemblrs587779193
gopubmedrs587779193
geneviewrs587779193
scholarrs587779193
googlers587779193
pharmgkbrs587779193
gwascentralrs587779193
openSNPrs587779193
23andMers587779193
23andMe allrs587779193
SNP Nexus

SNPshotrs587779193
SNPdbers587779193
MSV3drs587779193
GWAS Ctlgrs587779193
Max Magnitude0
ClinVar
Risk rs587779193(T;T)
Alt rs587779193(T;T)
Reference rs587779193(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641558G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076752.2,