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rs587779066

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779066(-;-)
Make rs587779066(-;A)
Make rs587779066(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47416371
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779066
ebirs587779066
HLIrs587779066
Exacrs587779066
Varsomers587779066
Maprs587779066
PheGenIrs587779066
hapmaprs587779066
1000 genomesrs587779066
hgdprs587779066
ensemblrs587779066
gopubmedrs587779066
geneviewrs587779066
scholarrs587779066
googlers587779066
pharmgkbrs587779066
gwascentralrs587779066
openSNPrs587779066
23andMers587779066
23andMe allrs587779066
SNP Nexus

SNPshotrs587779066
SNPdbers587779066
MSV3drs587779066
GWAS Ctlgrs587779066
Max Magnitude0
ClinVar
Risk rs587779066(A;A)
Alt rs587779066(A;A)
Reference rs587779066(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47643510dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076001.2,