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rs4950322

From SNPedia

Orientationplus
Stabilizedplus
Make rs4950322(A;A)
Make rs4950322(A;G)
Make rs4950322(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position147383114
GeneSEC24C
is asnp
is mentioned by
dbSNPrs4950322
ebirs4950322
HLIrs4950322
Exacrs4950322
Varsomers4950322
Maprs4950322
PheGenIrs4950322
hapmaprs4950322
1000 genomesrs4950322
hgdprs4950322
ensemblrs4950322
gopubmedrs4950322
geneviewrs4950322
scholarrs4950322
googlers4950322
pharmgkbrs4950322
gwascentralrs4950322
openSNPrs4950322
23andMers4950322
23andMe allrs4950322
SNP Nexus

SNPshotrs4950322
SNPdbers4950322
MSV3drs4950322
GWAS Ctlgrs4950322
GMAF0.1364
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18464913OA-icon.png]
Trait Protein quantitative trait loci
Title A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)
Risk Allele
P-val 6.9999999999999997E-7
Odds Ratio NR NR

[PMID 18464913OA-icon.png] Resistin (RETN) protein levels


GET Evidence
rs4950322
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.171875
summary