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rs267607754

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607754(-;-)
Make rs267607754(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37008848
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607754
ebirs267607754
HLIrs267607754
Exacrs267607754
Varsomers267607754
Maprs267607754
PheGenIrs267607754
hapmaprs267607754
1000 genomesrs267607754
hgdprs267607754
ensemblrs267607754
gopubmedrs267607754
geneviewrs267607754
scholarrs267607754
googlers267607754
pharmgkbrs267607754
gwascentralrs267607754
openSNPrs267607754
23andMers267607754
23andMe allrs267607754
SNP Nexus

SNPshotrs267607754
SNPdbers267607754
MSV3drs267607754
GWAS Ctlgrs267607754
Max Magnitude0
ClinVar
Risk rs267607754(;)
Alt rs267607754(;)
Reference rs267607754(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37050339delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075734.2,