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rs587779159

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779159(-;-)
Make rs587779159(-;T)
Make rs587779159(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47408541
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779159
ebirs587779159
HLIrs587779159
Exacrs587779159
Varsomers587779159
Maprs587779159
PheGenIrs587779159
hapmaprs587779159
1000 genomesrs587779159
hgdprs587779159
ensemblrs587779159
gopubmedrs587779159
geneviewrs587779159
scholarrs587779159
googlers587779159
pharmgkbrs587779159
gwascentralrs587779159
openSNPrs587779159
23andMers587779159
23andMe allrs587779159
SNP Nexus

SNPshotrs587779159
SNPdbers587779159
MSV3drs587779159
GWAS Ctlgrs587779159
Max Magnitude0
ClinVar
Risk rs587779159(T;T)
Alt rs587779159(T;T)
Reference rs587779159(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47635680dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076571.2,