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rs587778942

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587778942(-;-)
Make rs587778942(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37047532
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778942
ebirs587778942
HLIrs587778942
Exacrs587778942
Varsomers587778942
Maprs587778942
PheGenIrs587778942
hapmaprs587778942
1000 genomesrs587778942
hgdprs587778942
ensemblrs587778942
gopubmedrs587778942
geneviewrs587778942
scholarrs587778942
googlers587778942
pharmgkbrs587778942
gwascentralrs587778942
openSNPrs587778942
23andMers587778942
23andMe allrs587778942
SNP Nexus

SNPshotrs587778942
SNPdbers587778942
MSV3drs587778942
GWAS Ctlgrs587778942
Max Magnitude0
ClinVar
Risk rs587778942(;)
Alt rs587778942(;)
Reference rs587778942(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089023delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075348.2,