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rs587779149

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779149(-;-)
Make rs587779149(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47480782
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779149
ebirs587779149
HLIrs587779149
Exacrs587779149
Varsomers587779149
Maprs587779149
PheGenIrs587779149
hapmaprs587779149
1000 genomesrs587779149
hgdprs587779149
ensemblrs587779149
gopubmedrs587779149
geneviewrs587779149
scholarrs587779149
googlers587779149
pharmgkbrs587779149
gwascentralrs587779149
openSNPrs587779149
23andMers587779149
23andMe allrs587779149
SNP Nexus

SNPshotrs587779149
SNPdbers587779149
MSV3drs587779149
GWAS Ctlgrs587779149
Max Magnitude0
ClinVar
Risk rs587779149(;)
Alt rs587779149(;)
Reference rs587779149(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47707921delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076499.2,