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rs587779177

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779177(-;-)
Make rs587779177(-;C)
Make rs587779177(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47403264
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779177
ebirs587779177
HLIrs587779177
Exacrs587779177
Varsomers587779177
Maprs587779177
PheGenIrs587779177
hapmaprs587779177
1000 genomesrs587779177
hgdprs587779177
ensemblrs587779177
gopubmedrs587779177
geneviewrs587779177
scholarrs587779177
googlers587779177
pharmgkbrs587779177
gwascentralrs587779177
openSNPrs587779177
23andMers587779177
23andMe allrs587779177
SNP Nexus

SNPshotrs587779177
SNPdbers587779177
MSV3drs587779177
GWAS Ctlgrs587779177
Max Magnitude0
ClinVar
Risk rs587779177(C;C)
Alt rs587779177(C;C)
Reference rs587779177(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47630403_47630404insC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076697.2,