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rs587779131

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs587779131(-;-)
Make rs587779131(-;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47476407
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779131
ebirs587779131
HLIrs587779131
Exacrs587779131
Varsomers587779131
Maprs587779131
PheGenIrs587779131
hapmaprs587779131
1000 genomesrs587779131
hgdprs587779131
ensemblrs587779131
gopubmedrs587779131
geneviewrs587779131
scholarrs587779131
googlers587779131
pharmgkbrs587779131
gwascentralrs587779131
openSNPrs587779131
23andMers587779131
23andMe allrs587779131
SNP Nexus

SNPshotrs587779131
SNPdbers587779131
MSV3drs587779131
GWAS Ctlgrs587779131
Max Magnitude0
ClinVar
Risk rs587779131(;)
Alt rs587779131(;)
Reference rs587779131(TG;TG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703546_47703547delTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076369.2,