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rs587779106

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779106(-;-)
Make rs587779106(-;T)
Make rs587779106(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47471008
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779106
ebirs587779106
HLIrs587779106
Exacrs587779106
Varsomers587779106
Maprs587779106
PheGenIrs587779106
hapmaprs587779106
1000 genomesrs587779106
hgdprs587779106
ensemblrs587779106
gopubmedrs587779106
geneviewrs587779106
scholarrs587779106
googlers587779106
pharmgkbrs587779106
gwascentralrs587779106
openSNPrs587779106
23andMers587779106
23andMe allrs587779106
SNP Nexus

SNPshotrs587779106
SNPdbers587779106
MSV3drs587779106
GWAS Ctlgrs587779106
Max Magnitude0
ClinVar
Risk rs587779106(T;T)
Alt rs587779106(T;T)
Reference rs587779106(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698147_47698148insT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076255.2,