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rs587778926

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778926(-;-)
Make rs587778926(-;T)
Make rs587778926(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37028931
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778926
ebirs587778926
HLIrs587778926
Exacrs587778926
Varsomers587778926
Maprs587778926
PheGenIrs587778926
hapmaprs587778926
1000 genomesrs587778926
hgdprs587778926
ensemblrs587778926
gopubmedrs587778926
geneviewrs587778926
scholarrs587778926
googlers587778926
pharmgkbrs587778926
gwascentralrs587778926
openSNPrs587778926
23andMers587778926
23andMe allrs587778926
SNP Nexus

SNPshotrs587778926
SNPdbers587778926
MSV3drs587778926
GWAS Ctlgrs587778926
Max Magnitude0
ClinVar
Risk rs587778926(T;T)
Alt rs587778926(T;T)
Reference Rs587778926(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070422_37070423insT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075243.2,