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rs267607734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607734(A;A)
Make rs267607734(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37001054
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607734
ebirs267607734
HLIrs267607734
Exacrs267607734
Varsomers267607734
Maprs267607734
PheGenIrs267607734
hapmaprs267607734
1000 genomesrs267607734
hgdprs267607734
ensemblrs267607734
gopubmedrs267607734
geneviewrs267607734
scholarrs267607734
googlers267607734
pharmgkbrs267607734
gwascentralrs267607734
openSNPrs267607734
23andMers267607734
23andMe allrs267607734
SNP Nexus

SNPshotrs267607734
SNPdbers267607734
MSV3drs267607734
GWAS Ctlgrs267607734
Max Magnitude0
ClinVar
Risk rs267607734(A;A)
Alt rs267607734(A;A)
Reference rs267607734(G;G)
Significance Pathogenic
Disease Lynch syndrome I
Variation info
Gene MLH1
CLNDBN Lynch syndrome I
Reversed 0
HGVS NC_000003.11:g.37042545G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075628.3,