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rs267607852

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607852(A;T)
Make rs267607852(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047517
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607852
ebirs267607852
HLIrs267607852
Exacrs267607852
Varsomers267607852
Maprs267607852
PheGenIrs267607852
hapmaprs267607852
1000 genomesrs267607852
hgdprs267607852
ensemblrs267607852
gopubmedrs267607852
geneviewrs267607852
scholarrs267607852
googlers267607852
pharmgkbrs267607852
gwascentralrs267607852
openSNPrs267607852
23andMers267607852
23andMe allrs267607852
SNP Nexus

SNPshotrs267607852
SNPdbers267607852
MSV3drs267607852
GWAS Ctlgrs267607852
Max Magnitude0
ClinVar
Risk rs267607852(G,T;G,T)
Alt rs267607852(G,T;G,T)
Reference rs267607852(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089008A>G; NC_000003.11:g.37089008A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075335.2, RCV000075336.2,