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rs587779151

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATATC;ATATC) 0 common in clinvar
Make rs587779151(-;-)
Make rs587779151(-;ATCAT)
Make rs587779151(ATCAT;ATCAT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47480830
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779151
dbSNP (old)rs587779151
ClinGenrs587779151
ebirs587779151
HLIrs587779151
Exacrs587779151
Gnomadrs587779151
Varsomers587779151
Maprs587779151
PheGenIrs587779151
Biobankrs587779151
1000 genomesrs587779151
hgdprs587779151
ensemblrs587779151
gopubmedrs587779151
geneviewrs587779151
scholarrs587779151
googlers587779151
pharmgkbrs587779151
gwascentralrs587779151
openSNPrs587779151
23andMers587779151
23andMe allrs587779151
SNP Nexus

SNPshotrs587779151
SNPdbers587779151
MSV3drs587779151
GWAS Ctlgrs587779151
Max Magnitude0
ClinVar
Risk rs587779151(-;-)
Alt rs587779151(-;-)
Reference Rs587779151(ATATC;ATATC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47707969_47707973delATCAT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076511.2,