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rs587779147

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779147(-;-)
Make rs587779147(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47480758
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779147
ebirs587779147
HLIrs587779147
Exacrs587779147
Varsomers587779147
Maprs587779147
PheGenIrs587779147
hapmaprs587779147
1000 genomesrs587779147
hgdprs587779147
ensemblrs587779147
gopubmedrs587779147
geneviewrs587779147
scholarrs587779147
googlers587779147
pharmgkbrs587779147
gwascentralrs587779147
openSNPrs587779147
23andMers587779147
23andMe allrs587779147
SNP Nexus

SNPshotrs587779147
SNPdbers587779147
MSV3drs587779147
GWAS Ctlgrs587779147
Max Magnitude0
ClinVar
Risk rs587779147(;)
Alt rs587779147(;)
Reference rs587779147(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47707897delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076494.2,