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rs587779079

From SNPedia

Orientationplus
Geno Mag Summary
(ATGTT;ATGTT) 0 common in clinvar
Make rs587779079(-;-)
Make rs587779079(-;GTTAT)
Make rs587779079(GTTAT;GTTAT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47429914
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779079
ebirs587779079
HLIrs587779079
Exacrs587779079
Varsomers587779079
Maprs587779079
PheGenIrs587779079
hapmaprs587779079
1000 genomesrs587779079
hgdprs587779079
ensemblrs587779079
gopubmedrs587779079
geneviewrs587779079
scholarrs587779079
googlers587779079
pharmgkbrs587779079
gwascentralrs587779079
openSNPrs587779079
23andMers587779079
23andMe allrs587779079
SNP Nexus

SNPshotrs587779079
SNPdbers587779079
MSV3drs587779079
GWAS Ctlgrs587779079
Max Magnitude0
ClinVar
Risk rs587779079(;)
Alt rs587779079(;)
Reference rs587779079(ATGTT;ATGTT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47657053_47657057delGTTAT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076077.2,