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rs1039302

From SNPedia

Orientationplus
Stabilizedplus
Make rs1039302(C;C)
Make rs1039302(C;T)
Make rs1039302(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position120798455
GeneSPPL3
is asnp
is mentioned by
dbSNPrs1039302
ebirs1039302
HLIrs1039302
Exacrs1039302
Varsomers1039302
Maprs1039302
PheGenIrs1039302
hapmaprs1039302
1000 genomesrs1039302
hgdprs1039302
ensemblrs1039302
gopubmedrs1039302
geneviewrs1039302
scholarrs1039302
googlers1039302
pharmgkbrs1039302
gwascentralrs1039302
openSNPrs1039302
23andMers1039302
23andMe allrs1039302
SNP Nexus

SNPshotrs1039302
SNPdbers1039302
MSV3drs1039302
GWAS Ctlgrs1039302
GMAF0.3003
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19197348OA-icon.png]
Trait Quantitative traits
Title Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
Risk Allele T
P-val 0.000005
Odds Ratio 0.21 [NR] mg/L increase

C-reactive protein (CRP) levels being the quantitative trait associated with in [PMID 19197348OA-icon.png]


[PMID 18978678OA-icon.png] Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts.


GET Evidence
rs1039302
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.273438
summary