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rs587779191

From SNPedia

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Geno Mag Summary
(ACTG;ACTG) 0 common in clinvar
Make rs587779191(-;-)
Make rs587779191(-;GACT)
Make rs587779191(GACT;GACT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47414349
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779191
ebirs587779191
HLIrs587779191
Exacrs587779191
Varsomers587779191
Maprs587779191
PheGenIrs587779191
hapmaprs587779191
1000 genomesrs587779191
hgdprs587779191
ensemblrs587779191
gopubmedrs587779191
geneviewrs587779191
scholarrs587779191
googlers587779191
pharmgkbrs587779191
gwascentralrs587779191
openSNPrs587779191
23andMers587779191
23andMe allrs587779191
SNP Nexus

SNPshotrs587779191
SNPdbers587779191
MSV3drs587779191
GWAS Ctlgrs587779191
Max Magnitude0
ClinVar
Risk rs587779191(;)
Alt rs587779191(;)
Reference rs587779191(ACTG;ACTG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641488_47641491delGACT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076741.2,