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rs587779135

From SNPedia

Orientationplus
Geno Mag Summary
(TTGGGTGT;TTGGGTGT) 0 common in clinvar
Make rs587779135(-;-)
Make rs587779135(-;GGGTGTTT)
Make rs587779135(GGGTGTTT;GGGTGTTT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47476435
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779135
ebirs587779135
HLIrs587779135
Exacrs587779135
Varsomers587779135
Maprs587779135
PheGenIrs587779135
hapmaprs587779135
1000 genomesrs587779135
hgdprs587779135
ensemblrs587779135
gopubmedrs587779135
geneviewrs587779135
scholarrs587779135
googlers587779135
pharmgkbrs587779135
gwascentralrs587779135
openSNPrs587779135
23andMers587779135
23andMe allrs587779135
SNP Nexus

SNPshotrs587779135
SNPdbers587779135
MSV3drs587779135
GWAS Ctlgrs587779135
Max Magnitude0
ClinVar
Risk rs587779135(;)
Alt rs587779135(;)
Reference rs587779135(TTGGGTGT;TTGGGTGT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703574_47703581delGGGTGTTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076381.2,