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

rs267607773

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607773(-;-)
Make rs267607773(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37011863
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607773
ebirs267607773
HLIrs267607773
Exacrs267607773
Varsomers267607773
Maprs267607773
PheGenIrs267607773
hapmaprs267607773
1000 genomesrs267607773
hgdprs267607773
ensemblrs267607773
gopubmedrs267607773
geneviewrs267607773
scholarrs267607773
googlers267607773
pharmgkbrs267607773
gwascentralrs267607773
openSNPrs267607773
23andMers267607773
23andMe allrs267607773
SNP Nexus

SNPshotrs267607773
SNPdbers267607773
MSV3drs267607773
GWAS Ctlgrs267607773
Max Magnitude0
ClinVar
Risk rs267607773(;)
Alt rs267607773(;)
Reference rs267607773(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053354delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075770.2,