Have questions? Visit https://www.reddit.com/r/SNPedia

rs267607889

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607889(A;T)
Make rs267607889(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37050484
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607889
ebirs267607889
HLIrs267607889
Exacrs267607889
Varsomers267607889
Maprs267607889
PheGenIrs267607889
hapmaprs267607889
1000 genomesrs267607889
hgdprs267607889
ensemblrs267607889
gopubmedrs267607889
geneviewrs267607889
scholarrs267607889
googlers267607889
pharmgkbrs267607889
gwascentralrs267607889
openSNPrs267607889
23andMers267607889
23andMe allrs267607889
SNP Nexus

SNPshotrs267607889
SNPdbers267607889
MSV3drs267607889
GWAS Ctlgrs267607889
Max Magnitude0
ClinVar
Risk rs267607889(G,T;G,T)
Alt rs267607889(G,T;G,T)
Reference rs267607889(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37091975A>G; NC_000003.11:g.37091975A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075539.2, RCV000075540.2,