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rs587779103

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779103(-;-)
Make rs587779103(-;T)
Make rs587779103(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47470990
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779103
ebirs587779103
HLIrs587779103
Exacrs587779103
Varsomers587779103
Maprs587779103
PheGenIrs587779103
hapmaprs587779103
1000 genomesrs587779103
hgdprs587779103
ensemblrs587779103
gopubmedrs587779103
geneviewrs587779103
scholarrs587779103
googlers587779103
pharmgkbrs587779103
gwascentralrs587779103
openSNPrs587779103
23andMers587779103
23andMe allrs587779103
SNP Nexus

SNPshotrs587779103
SNPdbers587779103
MSV3drs587779103
GWAS Ctlgrs587779103
Max Magnitude0
ClinVar
Risk rs587779103(T;T)
Alt rs587779103(T;T)
Reference rs587779103(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698129dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076245.2,