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rs863225093

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225093(C;C)
Make rs863225093(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position144317794
GeneDGAT1, MIR6848
is asnp
is mentioned by
dbSNPrs863225093
ebirs863225093
HLIrs863225093
Exacrs863225093
Varsomers863225093
Maprs863225093
PheGenIrs863225093
hapmaprs863225093
1000 genomesrs863225093
hgdprs863225093
ensemblrs863225093
gopubmedrs863225093
geneviewrs863225093
scholarrs863225093
googlers863225093
pharmgkbrs863225093
gwascentralrs863225093
openSNPrs863225093
23andMers863225093
23andMe allrs863225093
SNP Nexus

SNPshotrs863225093
SNPdbers863225093
MSV3drs863225093
GWAS Ctlgrs863225093
Max Magnitude0
ClinVar
Risk rs863225093(C;C)
Alt rs863225093(C;C)
Reference rs863225093(T;T)
Significance Probable-Pathogenic
Disease Diarrhea 7
Variation info
Gene LOC101929012 DGAT1 MIR6848
CLNDBN Diarrhea 7
Reversed 1
HGVS NC_000008.10:g.145541457A>G
CLNSRC
CLNACC RCV000201459.1,