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rs267607896

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607896(-;-)
Make rs267607896(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37050606
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607896
ebirs267607896
HLIrs267607896
Exacrs267607896
Varsomers267607896
Maprs267607896
PheGenIrs267607896
hapmaprs267607896
1000 genomesrs267607896
hgdprs267607896
ensemblrs267607896
gopubmedrs267607896
geneviewrs267607896
scholarrs267607896
googlers267607896
pharmgkbrs267607896
gwascentralrs267607896
openSNPrs267607896
23andMers267607896
23andMe allrs267607896
SNP Nexus

SNPshotrs267607896
SNPdbers267607896
MSV3drs267607896
GWAS Ctlgrs267607896
Max Magnitude0
ClinVar
Risk rs267607896(;)
Alt rs267607896(;)
Reference rs267607896(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092097delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075582.2,