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rs587779104

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779104(A;T)
Make rs587779104(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47470996
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779104
ebirs587779104
HLIrs587779104
Exacrs587779104
Varsomers587779104
Maprs587779104
PheGenIrs587779104
hapmaprs587779104
1000 genomesrs587779104
hgdprs587779104
ensemblrs587779104
gopubmedrs587779104
geneviewrs587779104
scholarrs587779104
googlers587779104
pharmgkbrs587779104
gwascentralrs587779104
openSNPrs587779104
23andMers587779104
23andMe allrs587779104
SNP Nexus

SNPshotrs587779104
SNPdbers587779104
MSV3drs587779104
GWAS Ctlgrs587779104
Max Magnitude0
ClinVar
Risk rs587779104(T;T)
Alt rs587779104(T;T)
Reference rs587779104(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698135A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076248.2,