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rs587778911

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;T) 6 Lynch syndrome, pathogenic mutation
(T;T) 0 common in clinvar


Make rs587778911(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37026009
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778911
dbSNP (old)rs587778911
ClinGenrs587778911
ebirs587778911
HLIrs587778911
Exacrs587778911
Gnomadrs587778911
Varsomers587778911
Maprs587778911
PheGenIrs587778911
Biobankrs587778911
1000 genomesrs587778911
hgdprs587778911
ensemblrs587778911
gopubmedrs587778911
geneviewrs587778911
scholarrs587778911
googlers587778911
pharmgkbrs587778911
gwascentralrs587778911
openSNPrs587778911
23andMers587778911
23andMe allrs587778911
SNPshotrs587778911
SNPdbers587778911
MSV3drs587778911
GWAS Ctlgrs587778911
Max Magnitude6
ClinVar
Risk rs587778911(G;G)
Alt rs587778911(G;G)
Reference Rs587778911(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067500T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075194.2,