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rs587779176

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779176(-;-)
Make rs587779176(-;A)
Make rs587779176(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47412493
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779176
ebirs587779176
HLIrs587779176
Exacrs587779176
Varsomers587779176
Maprs587779176
PheGenIrs587779176
hapmaprs587779176
1000 genomesrs587779176
hgdprs587779176
ensemblrs587779176
gopubmedrs587779176
geneviewrs587779176
scholarrs587779176
googlers587779176
pharmgkbrs587779176
gwascentralrs587779176
openSNPrs587779176
23andMers587779176
23andMe allrs587779176
SNP Nexus

SNPshotrs587779176
SNPdbers587779176
MSV3drs587779176
GWAS Ctlgrs587779176
Max Magnitude0
ClinVar
Risk rs587779176(A;A)
Alt rs587779176(A;A)
Reference rs587779176(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639632dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076692.2,