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rs148665132

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs148665132(A;G)
Make rs148665132(G;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position144318093
GeneDGAT1, MIR6848
is asnp
is mentioned by
dbSNPrs148665132
dbSNP (classic)rs148665132
ClinGenrs148665132
ebirs148665132
HLIrs148665132
Exacrs148665132
Gnomadrs148665132
Varsomers148665132
LitVarrs148665132
Maprs148665132
PheGenIrs148665132
Biobankrs148665132
1000 genomesrs148665132
hgdprs148665132
ensemblrs148665132
geneviewrs148665132
scholarrs148665132
googlers148665132
pharmgkbrs148665132
gwascentralrs148665132
openSNPrs148665132
23andMers148665132
SNPshotrs148665132
SNPdbers148665132
MSV3drs148665132
GWAS Ctlgrs148665132
Max Magnitude0
ClinVar
Risk rs148665132(G;G)
Alt rs148665132(G;G)
Reference Rs148665132(A;A)
Significance Pathogenic
Disease Diarrhea 7
Variation info
Gene DGAT1 MIR6848
CLNDBN Diarrhea 7
Reversed 0
HGVS NC_000008.10:g.145541756A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000128413.2,