SNP Report

Basic Info

Name	rs1079597 dbSNP Ensembl
Location	chr11:113425564 - 113425564(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.250799
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000346454, ENST00000362072, ENST00000540600, ENST00000542616, ENST00000543292); non_coding_transcript_variant(ENST00000540600); upstream_gene_variant(ENST00000535984, ENST00000538967, ENST00000542968, ENST00000544518)
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)
DRD2	dopamine receptor D2	11q22-q23	28(8/20/0)

SNPs in LD with rs1079597 (count: 0) View in gBrowse (chr11:113425564..113425564 )

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

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