SNP Report

Basic Info

Name	rs931992 dbSNP Ensembl
Location	chr17:39665182 - 39665182(1)
Variant Alleles	G/T
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.466853
Functional Annotation	5_prime_UTR_variant; downstream_gene_variant; upstream_gene_variant.
Consequence to Transcript	5_prime_UTR_variant(ENST00000309889); downstream_gene_variant(ENST00000336308, ENST00000394250, ENST00000471896, ENST00000481171, ENST00000488876, ENST00000544210, ENST00000578384, ENST00000578577, ENST00000578686, ENST00000580611, ENST00000583639, ENST00000583884, ENST00000584850, ENST00000585269); upstream_gene_variant(ENST00000269582, ENST00000394246, ENST00000578283, ENST00000581428, LRG_210t1)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 3)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
STARD3	StAR-related lipid transfer (START) domain containing 3	17q11-q12	Mapped by Literature SNP
PNMT	phenylethanolamine N-methyltransferase	17q12	Mapped by LD-proxy
TCAP	titin-cap	17q12	Mapped by LD-proxy

SNPs in LD with rs931992 (count: 0) View in gBrowse (chr17:39665182..39665182 )

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

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