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rs267607758

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs267607758(-;-)
Make rs267607758(-;TT)
ReferenceGRCh38 38.1/141
Chromosome3
Position37008828
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607758
ebirs267607758
HLIrs267607758
Exacrs267607758
Varsomers267607758
Maprs267607758
PheGenIrs267607758
hapmaprs267607758
1000 genomesrs267607758
hgdprs267607758
ensemblrs267607758
gopubmedrs267607758
geneviewrs267607758
scholarrs267607758
googlers267607758
pharmgkbrs267607758
gwascentralrs267607758
openSNPrs267607758
23andMers267607758
23andMe allrs267607758
SNP Nexus

SNPshotrs267607758
SNPdbers267607758
MSV3drs267607758
GWAS Ctlgrs267607758
Max Magnitude0
ClinVar
Risk rs267607758(;)
Alt rs267607758(;)
Reference rs267607758(TT;TT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37050319_37050320delTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075731.2,