Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779188

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779188(-;-)
Make rs587779188(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47403273
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779188
ebirs587779188
HLIrs587779188
Exacrs587779188
Varsomers587779188
Maprs587779188
PheGenIrs587779188
hapmaprs587779188
1000 genomesrs587779188
hgdprs587779188
ensemblrs587779188
gopubmedrs587779188
geneviewrs587779188
scholarrs587779188
googlers587779188
pharmgkbrs587779188
gwascentralrs587779188
openSNPrs587779188
23andMers587779188
23andMe allrs587779188
SNP Nexus

SNPshotrs587779188
SNPdbers587779188
MSV3drs587779188
GWAS Ctlgrs587779188
Max Magnitude0
ClinVar
Risk rs587779188(;)
Alt rs587779188(;)
Reference rs587779188(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47630412delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076731.2,