SNP Report

Basic Info

Name	rs8092613 dbSNP Ensembl
Location	chr18:9182193 - 9182193(1)
Variant Alleles	T/A
Ancestral Allele	A
Minor Allele	T
Minor Allele Frequence	0.221446
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000262126, ENST00000400020, ENST00000540578, ENST00000577992, ENST00000578850, ENST00000579126, ENST00000581635, ENST00000585234); NMD_transcript_variant(ENST00000581635); non_coding_transcript_variant(ENST00000540578, ENST00000578850, ENST00000579126); upstream_gene_variant(ENST00000546007, ENST00000581758)
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)
ANKRD12	ankyrin repeat domain 12	18p11.22	Mapped by Literature SNP

SNPs in LD with rs8092613 (count: 0) View in gBrowse (chr18:9182193..9182193 )

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

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