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rs267607849

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;CTCA) 6 Lynch syndrome, pathogenic mutation
(ACTC;ACTC) 0 common in clinvar
(CTCA;CTCA) 0 common in clinvar


Make rs267607849(-;-)
ReferenceGRCh38 38.1/141
Chromosome3
Position37042290
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607849
dbSNP (old)rs267607849
ClinGenrs267607849
ebirs267607849
HLIrs267607849
Exacrs267607849
Gnomadrs267607849
Varsomers267607849
Maprs267607849
PheGenIrs267607849
Biobankrs267607849
1000 genomesrs267607849
hgdprs267607849
ensemblrs267607849
gopubmedrs267607849
geneviewrs267607849
scholarrs267607849
googlers267607849
pharmgkbrs267607849
gwascentralrs267607849
openSNPrs267607849
23andMers267607849
23andMe allrs267607849
SNP Nexus

SNPshotrs267607849
SNPdbers267607849
MSV3drs267607849
GWAS Ctlgrs267607849
Max Magnitude6
ClinVar
Risk rs267607849(-;-)
Alt rs267607849(-;-)
Reference Rs267607849(ACTC;ACTC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37083781_37083784delCTCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075315.2,