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

rs587779181

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779181(-;-)
Make rs587779181(-;CT)
Make rs587779181(CT;CT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47412536
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779181
ebirs587779181
HLIrs587779181
Exacrs587779181
Varsomers587779181
Maprs587779181
PheGenIrs587779181
hapmaprs587779181
1000 genomesrs587779181
hgdprs587779181
ensemblrs587779181
gopubmedrs587779181
geneviewrs587779181
scholarrs587779181
googlers587779181
pharmgkbrs587779181
gwascentralrs587779181
openSNPrs587779181
23andMers587779181
23andMe allrs587779181
SNP Nexus

SNPshotrs587779181
SNPdbers587779181
MSV3drs587779181
GWAS Ctlgrs587779181
Max Magnitude0
ClinVar
Risk rs587779181(CT;CT)
Alt rs587779181(CT;CT)
Reference rs587779181(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639674_47639675dupCT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076706.2,