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rs267607783

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
(TA;TA) 0 common in clinvar
Make rs267607783(-;-)
Make rs267607783(-;TA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37014429
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607783
ebirs267607783
HLIrs267607783
Exacrs267607783
Varsomers267607783
Maprs267607783
PheGenIrs267607783
hapmaprs267607783
1000 genomesrs267607783
hgdprs267607783
ensemblrs267607783
gopubmedrs267607783
geneviewrs267607783
scholarrs267607783
googlers267607783
pharmgkbrs267607783
gwascentralrs267607783
openSNPrs267607783
23andMers267607783
23andMe allrs267607783
SNP Nexus

SNPshotrs267607783
SNPdbers267607783
MSV3drs267607783
GWAS Ctlgrs267607783
Max Magnitude0
ClinVar
Risk rs267607783(;)
Alt rs267607783(;)
Reference rs267607783(AT;AT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37055920_37055921delTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075817.2,