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rs587779092

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779092(A;T)
Make rs587779092(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47463088
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779092
ebirs587779092
HLIrs587779092
Exacrs587779092
Varsomers587779092
Maprs587779092
PheGenIrs587779092
hapmaprs587779092
1000 genomesrs587779092
hgdprs587779092
ensemblrs587779092
gopubmedrs587779092
geneviewrs587779092
scholarrs587779092
googlers587779092
pharmgkbrs587779092
gwascentralrs587779092
openSNPrs587779092
23andMers587779092
23andMe allrs587779092
SNP Nexus

SNPshotrs587779092
SNPdbers587779092
MSV3drs587779092
GWAS Ctlgrs587779092
Max Magnitude0
ClinVar
Risk rs587779092(T;T)
Alt rs587779092(T;T)
Reference rs587779092(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690227A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076160.2,