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rs16996151

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs16996151(A;A)
Make rs16996151(A;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position89057649
GeneFAM13A
is asnp
is mentioned by
dbSNPrs16996151
ebirs16996151
HLIrs16996151
Exacrs16996151
Varsomers16996151
Maprs16996151
PheGenIrs16996151
hapmaprs16996151
1000 genomesrs16996151
hgdprs16996151
ensemblrs16996151
gopubmedrs16996151
geneviewrs16996151
scholarrs16996151
googlers16996151
pharmgkbrs16996151
gwascentralrs16996151
openSNPrs16996151
23andMers16996151
23andMe allrs16996151
SNP Nexus

SNPshotrs16996151
SNPdbers16996151
MSV3drs16996151
GWAS Ctlgrs16996151
GMAF0.01286
Max Magnitude0
? (A;A) (A;C) (C;C) 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 0.000006
Odds Ratio NR NR


GET Evidence
rs16996151
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.03125
summary