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rs17504622

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common genotype
Make rs17504622(C;T)
Make rs17504622(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position153274919
is asnp
is mentioned by
dbSNPrs17504622
dbSNP (classic)rs17504622
ClinGenrs17504622
ebirs17504622
HLIrs17504622
Exacrs17504622
Gnomadrs17504622
Varsomers17504622
LitVarrs17504622
Maprs17504622
PheGenIrs17504622
Biobankrs17504622
1000 genomesrs17504622
hgdprs17504622
ensemblrs17504622
geneviewrs17504622
scholarrs17504622
googlers17504622
pharmgkbrs17504622
gwascentralrs17504622
openSNPrs17504622
23andMers17504622
SNPshotrs17504622
SNPdbers17504622
MSV3drs17504622
GWAS Ctlgrs17504622
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23974872OA-icon.png]
Trait Schizophrenia
Title Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
Risk Allele T
P-val 3E-9
Odds Ratio 1.24 [1.17-1.31]