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rs587779152

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779152(A;A)
Make rs587779152(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47480859
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779152
ebirs587779152
HLIrs587779152
Exacrs587779152
Varsomers587779152
Maprs587779152
PheGenIrs587779152
hapmaprs587779152
1000 genomesrs587779152
hgdprs587779152
ensemblrs587779152
gopubmedrs587779152
geneviewrs587779152
scholarrs587779152
googlers587779152
pharmgkbrs587779152
gwascentralrs587779152
openSNPrs587779152
23andMers587779152
23andMe allrs587779152
SNP Nexus

SNPshotrs587779152
SNPdbers587779152
MSV3drs587779152
GWAS Ctlgrs587779152
Max Magnitude0
ClinVar
Risk rs587779152(A;A)
Alt rs587779152(A;A)
Reference rs587779152(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47707998T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076516.2,