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rs587779157

From SNPedia

Orientationplus
Geno Mag Summary
(AGTTGA;AGTTGA) 0 common in clinvar
Make rs587779157(-;-)
Make rs587779157(-;GAAGTT)
Make rs587779157(GAAGTT;GAAGTT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47408490
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779157
ebirs587779157
HLIrs587779157
Exacrs587779157
Varsomers587779157
Maprs587779157
PheGenIrs587779157
hapmaprs587779157
1000 genomesrs587779157
hgdprs587779157
ensemblrs587779157
gopubmedrs587779157
geneviewrs587779157
scholarrs587779157
googlers587779157
pharmgkbrs587779157
gwascentralrs587779157
openSNPrs587779157
23andMers587779157
23andMe allrs587779157
SNP Nexus

SNPshotrs587779157
SNPdbers587779157
MSV3drs587779157
GWAS Ctlgrs587779157
Max Magnitude0
ClinVar
Risk rs587779157(;)
Alt rs587779157(;)
Reference rs587779157(AGTTGA;AGTTGA)
Significance Probable-Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47635629_47635634delGAAGTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076562.2, RCV000129228.2, RCV000236396.1,