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rs1624802

From SNPedia

Orientationminus
Stabilizedminus
Make rs1624802(C;C)
Make rs1624802(C;T)
Make rs1624802(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position130012927
is asnp
is mentioned by
dbSNPrs1624802
dbSNP (classic)rs1624802
ClinGenrs1624802
ebirs1624802
HLIrs1624802
Exacrs1624802
Gnomadrs1624802
Varsomers1624802
LitVarrs1624802
Maprs1624802
PheGenIrs1624802
Biobankrs1624802
1000 genomesrs1624802
hgdprs1624802
ensemblrs1624802
geneviewrs1624802
scholarrs1624802
googlers1624802
pharmgkbrs1624802
gwascentralrs1624802
openSNPrs1624802
23andMers1624802
SNPshotrs1624802
SNPdbers1624802
MSV3drs1624802
GWAS Ctlgrs1624802
GMAF0.4536
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23251661OA-icon.png]
Trait Obesity-related traits
Title Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
Risk Allele A
P-val 5E-7
Odds Ratio .02 [NR] ng/dL increase