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rs587779148

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs587779148(-;-)
Make rs587779148(-;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47480762
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779148
dbSNP (old)rs587779148
ClinGenrs587779148
ebirs587779148
HLIrs587779148
Exacrs587779148
Varsomers587779148
Maprs587779148
PheGenIrs587779148
Biobankrs587779148
1000 genomesrs587779148
hgdprs587779148
ensemblrs587779148
gopubmedrs587779148
geneviewrs587779148
scholarrs587779148
googlers587779148
pharmgkbrs587779148
gwascentralrs587779148
openSNPrs587779148
23andMers587779148
23andMe allrs587779148
SNP Nexus

SNPshotrs587779148
SNPdbers587779148
MSV3drs587779148
GWAS Ctlgrs587779148
Max Magnitude0
ClinVar
Risk rs587779148(-;-)
Alt rs587779148(-;-)
Reference Rs587779148(AG;AG)
Significance Pathogenic
Disease Lynch syndrome Lynch syndrome I
Variation info
Gene MSH2
CLNDBN Lynch syndrome Lynch syndrome I
Reversed 0
HGVS NC_000002.11:g.47707901_47707902delAG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076495.2, RCV000410241.1,