SNP Report

Basic Info

Name	rs925994 dbSNP Ensembl
Location	chr16:85912411 - 85912411(1)
Variant Alleles	C/A
Ancestral Allele	C
Minor Allele	A
Minor Allele Frequence	0.102636
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000563180); intron_variant(ENST00000268638, ENST00000564056, ENST00000564617, ENST00000564803, ENST00000566369, LRG_294t1); non_coding_transcript_variant(ENST00000564056); upstream_gene_variant(ENST00000562492, ENST00000569145, ENST00000569607)
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)
IRF8	interferon regulatory factor 8	16q24.1	1(1/0/0)

SNPs in LD with rs925994 (count: 0) View in gBrowse (chr16:85912411..85912411 )

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

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