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

rs267607779

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607779(-;-)
Make rs267607779(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37012100
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607779
ebirs267607779
HLIrs267607779
Exacrs267607779
Varsomers267607779
Maprs267607779
PheGenIrs267607779
hapmaprs267607779
1000 genomesrs267607779
hgdprs267607779
ensemblrs267607779
gopubmedrs267607779
geneviewrs267607779
scholarrs267607779
googlers267607779
pharmgkbrs267607779
gwascentralrs267607779
openSNPrs267607779
23andMers267607779
23andMe allrs267607779
SNP Nexus

SNPshotrs267607779
SNPdbers267607779
MSV3drs267607779
GWAS Ctlgrs267607779
Max Magnitude0
ClinVar
Risk rs267607779(;)
Alt rs267607779(;)
Reference rs267607779(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053591delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075804.2,