SNP Report

Basic Info

Name	rs9609389 dbSNP Ensembl
Location	chr22:31939430 - 31939430(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.0976438
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000486651, ENST00000623735); non_coding_transcript_variant(ENST00000486651, ENST00000623735); upstream_gene_variant(ENST00000484682)
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)
C22orf24	chromosome 22 open reading frame 24	22q12.1-q12.3	Mapped by Literature SNP

SNPs in LD with rs9609389 (count: 0) View in gBrowse (chr22:31939430..31939430 )

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

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