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rs587778922

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778922(-;-)
Make rs587778922(-;T)
Make rs587778922(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36996655
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778922
ebirs587778922
HLIrs587778922
Exacrs587778922
Varsomers587778922
Maprs587778922
PheGenIrs587778922
hapmaprs587778922
1000 genomesrs587778922
hgdprs587778922
ensemblrs587778922
gopubmedrs587778922
geneviewrs587778922
scholarrs587778922
googlers587778922
pharmgkbrs587778922
gwascentralrs587778922
openSNPrs587778922
23andMers587778922
23andMe allrs587778922
SNP Nexus

SNPshotrs587778922
SNPdbers587778922
MSV3drs587778922
GWAS Ctlgrs587778922
Max Magnitude0
ClinVar
Risk rs587778922(T;T)
Alt rs587778922(T;T)
Reference rs587778922(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038146dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075237.2,