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rs267607735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607735(A;A)
Make rs267607735(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37001058
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607735
ebirs267607735
HLIrs267607735
Exacrs267607735
Varsomers267607735
Maprs267607735
PheGenIrs267607735
hapmaprs267607735
1000 genomesrs267607735
hgdprs267607735
ensemblrs267607735
gopubmedrs267607735
geneviewrs267607735
scholarrs267607735
googlers267607735
pharmgkbrs267607735
gwascentralrs267607735
openSNPrs267607735
23andMers267607735
23andMe allrs267607735
SNP Nexus

SNPshotrs267607735
SNPdbers267607735
MSV3drs267607735
GWAS Ctlgrs267607735
Max Magnitude0
ClinVar
Risk rs267607735(A;A)
Alt rs267607735(A;A)
Reference rs267607735(G;G)
Significance Pathogenic
Disease Lynch syndrome II Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome II Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37042549G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours OMIM Allelic Variant
CLNACC RCV000022504.27, RCV000075634.2, RCV000202186.1,