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rs267607755

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607755(A;A)
Make rs267607755(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37008857
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607755
ebirs267607755
HLIrs267607755
Exacrs267607755
Varsomers267607755
Maprs267607755
PheGenIrs267607755
hapmaprs267607755
1000 genomesrs267607755
hgdprs267607755
ensemblrs267607755
gopubmedrs267607755
geneviewrs267607755
scholarrs267607755
googlers267607755
pharmgkbrs267607755
gwascentralrs267607755
openSNPrs267607755
23andMers267607755
23andMe allrs267607755
SNP Nexus

SNPshotrs267607755
SNPdbers267607755
MSV3drs267607755
GWAS Ctlgrs267607755
Max Magnitude0
ClinVar
Risk rs267607755(A;A)
Alt rs267607755(A;A)
Reference rs267607755(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37050348T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075735.2,