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rs1520223

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs1520223(A;G)
Make rs1520223(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position102332560
is asnp
is mentioned by
dbSNPrs1520223
ebirs1520223
HLIrs1520223
Exacrs1520223
Varsomers1520223
Maprs1520223
PheGenIrs1520223
hapmaprs1520223
1000 genomesrs1520223
hgdprs1520223
ensemblrs1520223
gopubmedrs1520223
geneviewrs1520223
scholarrs1520223
googlers1520223
pharmgkbrs1520223
gwascentralrs1520223
openSNPrs1520223
23andMers1520223
23andMe allrs1520223
SNP Nexus

SNPshotrs1520223
SNPdbers1520223
MSV3drs1520223
GWAS Ctlgrs1520223
GMAF0.08953
Max Magnitude0
? (A;A) (A;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 9E-7
Odds Ratio 0.56 [NR] cm decrease


GET Evidence
rs1520223
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0234375
summary