SNP Report

Basic Info

Name	rs6866255 dbSNP Ensembl
Location	chr5:102480623 - 102480623(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.407348
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000379807, ENST00000389019, ENST00000505407, ENST00000506729, ENST00000513675, ENST00000514551); non_coding_transcript_variant(ENST00000505407, ENST00000514551); upstream_gene_variant(ENST00000505739)
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 rs6866255 (count: 0) View in gBrowse (chr5:102480623..102480623 )

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

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