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rs587779140

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779140(-;-)
Make rs587779140(-;T)
Make rs587779140(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47476528
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779140
ebirs587779140
HLIrs587779140
Exacrs587779140
Varsomers587779140
Maprs587779140
PheGenIrs587779140
hapmaprs587779140
1000 genomesrs587779140
hgdprs587779140
ensemblrs587779140
gopubmedrs587779140
geneviewrs587779140
scholarrs587779140
googlers587779140
pharmgkbrs587779140
gwascentralrs587779140
openSNPrs587779140
23andMers587779140
23andMe allrs587779140
SNP Nexus

SNPshotrs587779140
SNPdbers587779140
MSV3drs587779140
GWAS Ctlgrs587779140
Max Magnitude0
ClinVar
Risk rs587779140(T;T)
Alt rs587779140(T;T)
Reference rs587779140(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703667dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076414.2,