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rs267607799

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATCG;ATCG) 0 common in clinvar
(GATC;GATC) 0 common in clinvar
Make rs267607799(-;-)
Make rs267607799(-;ATCG)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017506
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607799
ebirs267607799
HLIrs267607799
Exacrs267607799
Varsomers267607799
Maprs267607799
PheGenIrs267607799
hapmaprs267607799
1000 genomesrs267607799
hgdprs267607799
ensemblrs267607799
gopubmedrs267607799
geneviewrs267607799
scholarrs267607799
googlers267607799
pharmgkbrs267607799
gwascentralrs267607799
openSNPrs267607799
23andMers267607799
23andMe allrs267607799
SNP Nexus

SNPshotrs267607799
SNPdbers267607799
MSV3drs267607799
GWAS Ctlgrs267607799
Max Magnitude0
ClinVar
Risk rs267607799(;)
Alt rs267607799(;)
Reference rs267607799(GATC;GATC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37058997_37059000delATCG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075870.2,