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

rs267607871

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607871(A;G)
Make rs267607871(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048515
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607871
ebirs267607871
HLIrs267607871
Exacrs267607871
Varsomers267607871
Maprs267607871
PheGenIrs267607871
hapmaprs267607871
1000 genomesrs267607871
hgdprs267607871
ensemblrs267607871
gopubmedrs267607871
geneviewrs267607871
scholarrs267607871
googlers267607871
pharmgkbrs267607871
gwascentralrs267607871
openSNPrs267607871
23andMers267607871
23andMe allrs267607871
SNP Nexus

SNPshotrs267607871
SNPdbers267607871
MSV3drs267607871
GWAS Ctlgrs267607871
Max Magnitude0
ClinVar
Risk rs267607871(G;G)
Alt rs267607871(G;G)
Reference rs267607871(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090006A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075411.2,