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rs17119280

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs17119280(A;A)
Make rs17119280(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position59333489
GeneFGGY
is asnp
is mentioned by
dbSNPrs17119280
ebirs17119280
HLIrs17119280
Exacrs17119280
Varsomers17119280
Maprs17119280
PheGenIrs17119280
hapmaprs17119280
1000 genomesrs17119280
hgdprs17119280
ensemblrs17119280
gopubmedrs17119280
geneviewrs17119280
scholarrs17119280
googlers17119280
pharmgkbrs17119280
gwascentralrs17119280
openSNPrs17119280
23andMers17119280
23andMe allrs17119280
SNP Nexus

SNPshotrs17119280
SNPdbers17119280
MSV3drs17119280
GWAS Ctlgrs17119280
GMAF0.0225
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19875103OA-icon.png]
Trait Response to antipsychotic therapy (extrapyramidal side effects)
Title Genomewide Association Study of Movement-Related Adverse Antipsychotic Effects
Risk Allele
P-val 0.000007
Odds Ratio NR NR


GET Evidence
rs17119280
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0234375
summary