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rs587779145

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779145(A;T)
Make rs587779145(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47408433
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779145
ebirs587779145
HLIrs587779145
Exacrs587779145
Varsomers587779145
Maprs587779145
PheGenIrs587779145
hapmaprs587779145
1000 genomesrs587779145
hgdprs587779145
ensemblrs587779145
gopubmedrs587779145
geneviewrs587779145
scholarrs587779145
googlers587779145
pharmgkbrs587779145
gwascentralrs587779145
openSNPrs587779145
23andMers587779145
23andMe allrs587779145
SNP Nexus

SNPshotrs587779145
SNPdbers587779145
MSV3drs587779145
GWAS Ctlgrs587779145
Max Magnitude0
ClinVar
Risk rs587779145(T;T)
Alt rs587779145(T;T)
Reference rs587779145(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47635572A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076477.2,