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

rs267607759

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607759(A;G)
Make rs267607759(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37011818
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607759
ebirs267607759
HLIrs267607759
Exacrs267607759
Varsomers267607759
Maprs267607759
PheGenIrs267607759
hapmaprs267607759
1000 genomesrs267607759
hgdprs267607759
ensemblrs267607759
gopubmedrs267607759
geneviewrs267607759
scholarrs267607759
googlers267607759
pharmgkbrs267607759
gwascentralrs267607759
openSNPrs267607759
23andMers267607759
23andMe allrs267607759
SNP Nexus

SNPshotrs267607759
SNPdbers267607759
MSV3drs267607759
GWAS Ctlgrs267607759
Max Magnitude0
ClinVar
Risk rs267607759(C,G;C,G)
Alt rs267607759(C,G;C,G)
Reference rs267607759(A;A)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37053309A>C; NC_000003.11:g.37053309A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075755.2, RCV000075756.2, RCV000202027.1,