Have questions? Visit https://www.reddit.com/r/SNPedia

rs17690232

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17690232(C;G)
Make rs17690232(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position54368658
is asnp
is mentioned by
dbSNPrs17690232
ebirs17690232
HLIrs17690232
Exacrs17690232
Varsomers17690232
Maprs17690232
PheGenIrs17690232
hapmaprs17690232
1000 genomesrs17690232
hgdprs17690232
ensemblrs17690232
gopubmedrs17690232
geneviewrs17690232
scholarrs17690232
googlers17690232
pharmgkbrs17690232
gwascentralrs17690232
openSNPrs17690232
23andMers17690232
23andMe allrs17690232
SNP Nexus

SNPshotrs17690232
SNPdbers17690232
MSV3drs17690232
GWAS Ctlgrs17690232
GMAF0.09642
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS
SNP rs17690232
PubMedID [PMID 18193045OA-icon.png]
Condition Height
Gene PDGFRA
Risk Allele C
pValue 4.00E-007
OR 0.86
95% CI NR) cm talle



GET Evidence
rs17690232
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.132812
summary