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rs267607699

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267607699(-;-)
Make rs267607699(-;AAGT)
Make rs267607699(AAGT;AAGT)
ReferenceGRCh38 38.1/141
Chromosome3
Position37040291
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607699
ebirs267607699
HLIrs267607699
Exacrs267607699
Varsomers267607699
Maprs267607699
PheGenIrs267607699
hapmaprs267607699
1000 genomesrs267607699
hgdprs267607699
ensemblrs267607699
gopubmedrs267607699
geneviewrs267607699
scholarrs267607699
googlers267607699
pharmgkbrs267607699
gwascentralrs267607699
openSNPrs267607699
23andMers267607699
23andMe allrs267607699
SNP Nexus

SNPshotrs267607699
SNPdbers267607699
MSV3drs267607699
GWAS Ctlgrs267607699
Max Magnitude0
ClinVar
Risk rs267607699(TAAG;TAAG)
Alt rs267607699(TAAG;TAAG)
Reference rs267607699(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081782_37081783insAAGT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075297.2,