SNP Report

Basic Info

Name	rs12907966 dbSNP Ensembl
Location	chr15:78550709 - 78550709(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.226238
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000044462); downstream_gene_variant(ENST00000413382, ENST00000557929, ENST00000558094, ENST00000558281, ENST00000558341, ENST00000559082, ENST00000559146, ENST00000559154, ENST00000559365, ENST00000559437, ENST00000559934, ENST00000559948, ENST00000560099, ENST00000560217, ENST00000560737)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
PSMA4	proteasome (prosome, macropain) subunit, alpha type, 4	15q24.1	Mapped by Literature SNP

SNPs in LD with rs12907966 (count: 0) View in gBrowse (chr15:78550709..78550709 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)