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rs267607788

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607788(G;G)
Make rs267607788(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017501
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607788
ebirs267607788
HLIrs267607788
Exacrs267607788
Varsomers267607788
Maprs267607788
PheGenIrs267607788
hapmaprs267607788
1000 genomesrs267607788
hgdprs267607788
ensemblrs267607788
gopubmedrs267607788
geneviewrs267607788
scholarrs267607788
googlers267607788
pharmgkbrs267607788
gwascentralrs267607788
openSNPrs267607788
23andMers267607788
23andMe allrs267607788
SNP Nexus

SNPshotrs267607788
SNPdbers267607788
MSV3drs267607788
GWAS Ctlgrs267607788
Max Magnitude0
ClinVar
Risk rs267607788(G;G)
Alt rs267607788(G;G)
Reference rs267607788(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37058992T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075865.2,