SNP Report

Basic Info

Name	rs6596482 dbSNP Ensembl
Location	chr5:102400937 - 102400937(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.420128
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000379807, ENST00000389019, ENST00000506729, ENST00000513675)
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)
SLCO6A1	solute carrier organic anion transporter family, member 6A1	5q21.2	Mapped by Literature SNP

SNPs in LD with rs6596482 (count: 0) View in gBrowse (chr5:102400937..102400937 )

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

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