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rs1435703

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1435703(G;T)
Make rs1435703(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position25518740
GeneRARB
is asnp
is mentioned by
dbSNPrs1435703
ebirs1435703
HLIrs1435703
Exacrs1435703
Varsomers1435703
Maprs1435703
PheGenIrs1435703
hapmaprs1435703
1000 genomesrs1435703
hgdprs1435703
ensemblrs1435703
gopubmedrs1435703
geneviewrs1435703
scholarrs1435703
googlers1435703
pharmgkbrs1435703
gwascentralrs1435703
openSNPrs1435703
23andMers1435703
23andMe allrs1435703
SNP Nexus

SNPshotrs1435703
SNPdbers1435703
MSV3drs1435703
GWAS Ctlgrs1435703
GMAF0.1368
Max Magnitude0
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19553259OA-icon.png]
Trait Obesity (extreme)
Title Common BMI-associated variants confer risk of extreme obesity
Risk Allele T
P-val 0.000004
Odds Ratio 1.66 [1.34-2.06]


GET Evidence
rs1435703
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.195312
summary