SNP Report

Basic Info

Name	rs9963823 dbSNP Ensembl
Location	chr18:56755538 - 56755538(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.0153754
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000254442, ENST00000357574, ENST00000585824, ENST00000587403, ENST00000589935, ENST00000590557, ENST00000615645); non_coding_transcript_variant(ENST00000585824, ENST00000587403, ENST00000590557); upstream_gene_variant(ENST00000384138, ENST00000591524)
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)
WDR7	WD repeat domain 7	18q21.31	1(0/1/0)

SNPs in LD with rs9963823 (count: 0) View in gBrowse (chr18:56755538..56755538 )

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

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