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rs267607765

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607765(A;A)
Make rs267607765(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37008906
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607765
ebirs267607765
HLIrs267607765
Exacrs267607765
Varsomers267607765
Maprs267607765
PheGenIrs267607765
hapmaprs267607765
1000 genomesrs267607765
hgdprs267607765
ensemblrs267607765
gopubmedrs267607765
geneviewrs267607765
scholarrs267607765
googlers267607765
pharmgkbrs267607765
gwascentralrs267607765
openSNPrs267607765
23andMers267607765
23andMe allrs267607765
SNP Nexus

SNPshotrs267607765
SNPdbers267607765
MSV3drs267607765
GWAS Ctlgrs267607765
Max Magnitude0
ClinVar
Risk rs267607765(A;A)
Alt rs267607765(A;A)
Reference rs267607765(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37050397G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075748.2,