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rs587779129

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs587779129(-;-)
Make rs587779129(-;AT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47476396
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779129
ebirs587779129
HLIrs587779129
Exacrs587779129
Varsomers587779129
Maprs587779129
PheGenIrs587779129
hapmaprs587779129
1000 genomesrs587779129
hgdprs587779129
ensemblrs587779129
gopubmedrs587779129
geneviewrs587779129
scholarrs587779129
googlers587779129
pharmgkbrs587779129
gwascentralrs587779129
openSNPrs587779129
23andMers587779129
23andMe allrs587779129
SNP Nexus

SNPshotrs587779129
SNPdbers587779129
MSV3drs587779129
GWAS Ctlgrs587779129
Max Magnitude0
ClinVar
Risk rs587779129(;)
Alt rs587779129(;)
Reference rs587779129(AT;AT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703535_47703536delAT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076367.2,