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rs267607866

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;G) 6 Lynch syndrome, pathogenic mutation
(G;G) 0 common in clinvar


Make rs267607866(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position37047642
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607866
dbSNP (old)rs267607866
ClinGenrs267607866
ebirs267607866
HLIrs267607866
Exacrs267607866
Gnomadrs267607866
Varsomers267607866
LitVarrs267607866
Maprs267607866
PheGenIrs267607866
Biobankrs267607866
1000 genomesrs267607866
hgdprs267607866
ensemblrs267607866
gopubmedrs267607866
geneviewrs267607866
scholarrs267607866
googlers267607866
pharmgkbrs267607866
gwascentralrs267607866
openSNPrs267607866
23andMers267607866
23andMe allrs267607866
SNPshotrs267607866
SNPdbers267607866
MSV3drs267607866
GWAS Ctlgrs267607866
Max Magnitude6
ClinVar
Risk rs267607866(C;C)
Alt rs267607866(C;C)
Reference Rs267607866(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome I Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome I Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37089133G>C
CLNSRC UniProtKB (protein)
CLNACC RCV000075387.2, RCV000165622.1,