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rs5749482

From SNPedia

Orientationplus
Stabilizedplus
Make rs5749482(C;C)
Make rs5749482(C;G)
Make rs5749482(G;G)
ReferenceGRCh37.p5 37.3/135
Chromosome22
Position32663679
GeneLOC105373002, SYN3
is asnp
is mentioned by
dbSNPrs5749482
dbSNP (classic)rs5749482
ClinGenrs5749482
ebirs5749482
HLIrs5749482
Exacrs5749482
Gnomadrs5749482
Varsomers5749482
LitVarrs5749482
Maprs5749482
PheGenIrs5749482
Biobankrs5749482
1000 genomesrs5749482
hgdprs5749482
ensemblrs5749482
geneviewrs5749482
scholarrs5749482
googlers5749482
pharmgkbrs5749482
gwascentralrs5749482
openSNPrs5749482
23andMers5749482
SNPshotrs5749482
SNPdbers5749482
MSV3drs5749482
GWAS Ctlgrs5749482
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GWAS snp
PMID [PMID 21998595OA-icon.png]
Trait
Title Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry.
Risk Allele C
P-val 5E-7
Odds Ratio 0.0400 None
GWAS snp
PMID [PMID 23455636OA-icon.png]
Trait Age-related macular degeneration
Title Seven new loci associated with age-related macular degeneration.
Risk Allele G
P-val 2E-26
Odds Ratio 1.31 [1.26-1.36]