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rs267607728

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607728(-;-)
Make rs267607728(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37001008
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607728
ebirs267607728
HLIrs267607728
Exacrs267607728
Varsomers267607728
Maprs267607728
PheGenIrs267607728
hapmaprs267607728
1000 genomesrs267607728
hgdprs267607728
ensemblrs267607728
gopubmedrs267607728
geneviewrs267607728
scholarrs267607728
googlers267607728
pharmgkbrs267607728
gwascentralrs267607728
openSNPrs267607728
23andMers267607728
23andMe allrs267607728
SNP Nexus

SNPshotrs267607728
SNPdbers267607728
MSV3drs267607728
GWAS Ctlgrs267607728
Max Magnitude0
ClinVar
Risk rs267607728(;)
Alt rs267607728(;)
Reference rs267607728(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37042499delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075609.2,