SNP Report

Basic Info

Name	rs7174513 dbSNP Ensembl
Location	chr15:41019743 - 41019743(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.139577
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000361937, ENST00000401393, ENST00000557849, ENST00000558357, ENST00000558967, ENST00000616814); NMD_transcript_variant(ENST00000557849, ENST00000558357); non_coding_transcript_variant(ENST00000558967); upstream_gene_variant(ENST00000560178, ENST00000624853)
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)
INO80	INO80 complex subunit	15q15.1	1(0/1/0)

SNPs in LD with rs7174513 (count: 0) View in gBrowse (chr15:41019743..41019743 )

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

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