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rs587779144

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779144(-;-)
Make rs587779144(-;C)
Make rs587779144(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47478479
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779144
ebirs587779144
HLIrs587779144
Exacrs587779144
Varsomers587779144
Maprs587779144
PheGenIrs587779144
hapmaprs587779144
1000 genomesrs587779144
hgdprs587779144
ensemblrs587779144
gopubmedrs587779144
geneviewrs587779144
scholarrs587779144
googlers587779144
pharmgkbrs587779144
gwascentralrs587779144
openSNPrs587779144
23andMers587779144
23andMe allrs587779144
SNP Nexus

SNPshotrs587779144
SNPdbers587779144
MSV3drs587779144
GWAS Ctlgrs587779144
Max Magnitude0
ClinVar
Risk rs587779144(C;C)
Alt rs587779144(C;C)
Reference rs587779144(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705618dupC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076469.2,