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rs267607906

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607906(A;T)
Make rs267607906(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37050576
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607906
ebirs267607906
HLIrs267607906
Exacrs267607906
Varsomers267607906
Maprs267607906
PheGenIrs267607906
hapmaprs267607906
1000 genomesrs267607906
hgdprs267607906
ensemblrs267607906
gopubmedrs267607906
geneviewrs267607906
scholarrs267607906
googlers267607906
pharmgkbrs267607906
gwascentralrs267607906
openSNPrs267607906
23andMers267607906
23andMe allrs267607906
SNP Nexus

SNPshotrs267607906
SNPdbers267607906
MSV3drs267607906
GWAS Ctlgrs267607906
Max Magnitude0
ClinVar
Risk rs267607906(T;T)
Alt rs267607906(T;T)
Reference rs267607906(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092067A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075573.2,