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rs2292303

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2292303(C;C)
Make rs2292303(C;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position102119753
GeneC12orf48, NUP37
is asnp
is mentioned by
dbSNPrs2292303
ebirs2292303
HLIrs2292303
Exacrs2292303
Varsomers2292303
Maprs2292303
PheGenIrs2292303
hapmaprs2292303
1000 genomesrs2292303
hgdprs2292303
ensemblrs2292303
gopubmedrs2292303
geneviewrs2292303
scholarrs2292303
googlers2292303
pharmgkbrs2292303
gwascentralrs2292303
openSNPrs2292303
23andMers2292303
23andMe allrs2292303
SNP Nexus

SNPshotrs2292303
SNPdbers2292303
MSV3drs2292303
GWAS Ctlgrs2292303
GMAF0.1024
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19893584]
Trait Height
Title Identification of 15 loci influencing height in a Korean population
Risk Allele C
P-val 0.000008
Odds Ratio 0.51 [NR] cm decrease


GET Evidence
rs2292303
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0390625
summary