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rs587779111

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779111(-;-)
Make rs587779111(-;A)
Make rs587779111(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47475052
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779111
ebirs587779111
HLIrs587779111
Exacrs587779111
Varsomers587779111
Maprs587779111
PheGenIrs587779111
hapmaprs587779111
1000 genomesrs587779111
hgdprs587779111
ensemblrs587779111
gopubmedrs587779111
geneviewrs587779111
scholarrs587779111
googlers587779111
pharmgkbrs587779111
gwascentralrs587779111
openSNPrs587779111
23andMers587779111
23andMe allrs587779111
SNP Nexus

SNPshotrs587779111
SNPdbers587779111
MSV3drs587779111
GWAS Ctlgrs587779111
Max Magnitude0
ClinVar
Risk rs587779111(A;A)
Alt rs587779111(A;A)
Reference rs587779111(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702191dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076287.2,