SNP Report

Basic Info

Name	rs17059456 dbSNP Ensembl
Location	chr8:28798414 - 28798414(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.235224
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000416984, ENST00000518510, ENST00000520983, ENST00000521022, ENST00000521777, ENST00000522363, ENST00000523303, ENST00000523436, ENST00000524081); NMD_transcript_variant(ENST00000518510, ENST00000522363, ENST00000523303); non_coding_transcript_exon_variant(ENST00000520055); non_coding_transcript_variant(ENST00000520055, ENST00000520983); upstream_gene_variant(ENST00000522074)
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)
INTS9	integrator complex subunit 9	8p21.1	1(1/0/0)

SNPs in LD with rs17059456 (count: 0) View in gBrowse (chr8:28798414..28798414 )

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

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