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rs2304796

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2304796(C;T)
Make rs2304796(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position89667026
GenePLIN1
is asnp
is mentioned by
dbSNPrs2304796
dbSNP (classic)rs2304796
ClinGenrs2304796
ebirs2304796
HLIrs2304796
Exacrs2304796
Gnomadrs2304796
Varsomers2304796
LitVarrs2304796
Maprs2304796
PheGenIrs2304796
Biobankrs2304796
1000 genomesrs2304796
hgdprs2304796
ensemblrs2304796
geneviewrs2304796
scholarrs2304796
googlers2304796
pharmgkbrs2304796
gwascentralrs2304796
openSNPrs2304796
23andMers2304796
SNPshotrs2304796
SNPdbers2304796
MSV3drs2304796
GWAS Ctlgrs2304796
Max Magnitude0

[PMID 23517113] Association between three genetic variants of the Perilipin Gene (PLIN) and glucose metabolism: results from a replication study among Chinese adults and a meta-analysis

ClinVar
Risk rs2304796(G;G) rs2304796(T;T)
Alt rs2304796(G;G) rs2304796(T;T)
Reference Rs2304796(C;C)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene PLIN1
CLNDBN not specified
Reversed 1
HGVS NC_000015.9:g.90210257G>A
CLNSRC ClinVar University of Chicago
CLNACC RCV000117992.2,