SNP Report

Basic Info

Name	rs3093988 dbSNP Ensembl
Location	chrCHR_HSCHR6_MHC_SSTO_CTG1:31515424 - 31515424(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.081869
Functional Annotation	upstream_gene_variant.
Consequence to Transcript	upstream_gene_variant(ENST00000376191, ENST00000403866, ENST00000416625, ENST00000424816, ENST00000440658, ENST00000450413, ENST00000417590, ENST00000421209, ENST00000443635, ENST00000447554, ENST00000452195, ENST00000456043, ENST00000419391, ENST00000420447, ENST00000443405, ENST00000430073, ENST00000443254, ENST00000451666, ENST00000383512, ENST00000418291, ENST00000457032, ENST00000422733, ENST00000442288, ENST00000445480)
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)
PPIAP9	peptidylprolyl isomerase A (cyclophilin A) pseudogene 9	6p21.3	Mapped by LD-proxy

SNPs in LD with rs3093988 (count: 0) View in gBrowse (chrCHR_HSCHR6_MHC_SSTO_CTG1:31515424..31515424 )

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

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