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rs267607774

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGTC;AGTC) 0 common in clinvar
Make rs267607774(-;-)
Make rs267607774(-;AGTC)
ReferenceGRCh38 38.1/141
Chromosome3
Position37012095
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607774
ebirs267607774
HLIrs267607774
Exacrs267607774
Varsomers267607774
Maprs267607774
PheGenIrs267607774
hapmaprs267607774
1000 genomesrs267607774
hgdprs267607774
ensemblrs267607774
gopubmedrs267607774
geneviewrs267607774
scholarrs267607774
googlers267607774
pharmgkbrs267607774
gwascentralrs267607774
openSNPrs267607774
23andMers267607774
23andMe allrs267607774
SNP Nexus

SNPshotrs267607774
SNPdbers267607774
MSV3drs267607774
GWAS Ctlgrs267607774
Max Magnitude0
ClinVar
Risk rs267607774(;)
Alt rs267607774(;)
Reference rs267607774(AGTC;AGTC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053586_37053589delAGTC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075800.2,