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rs587778978

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 6 Lynch syndrome, pathogenic mutation
Make rs587778978(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37050485
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778978
dbSNP (old)rs587778978
ClinGenrs587778978
ebirs587778978
HLIrs587778978
Exacrs587778978
Gnomadrs587778978
Varsomers587778978
Maprs587778978
PheGenIrs587778978
Biobankrs587778978
1000 genomesrs587778978
hgdprs587778978
ensemblrs587778978
gopubmedrs587778978
geneviewrs587778978
scholarrs587778978
googlers587778978
pharmgkbrs587778978
gwascentralrs587778978
openSNPrs587778978
23andMers587778978
23andMe allrs587778978
SNPshotrs587778978
SNPdbers587778978
MSV3drs587778978
GWAS Ctlgrs587778978
Max Magnitude6
ClinVar
Risk rs587778978(T;T)
Alt rs587778978(T;T)
Reference Rs587778978(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37091976G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075537.2,