SNP Report

Basic Info

Name	rs1517618 dbSNP Ensembl
Location	chr15:92104415 - 92104415(1)
Variant Alleles	G/C
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.0974441
Functional Annotation	missense_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant. Polyphen Annotation: benign(ENST00000318445, ENST00000424469) SIFT Annotation: tolerated(ENST00000318445, ENST00000424469)
Consequence to Transcript	missense_variant(ENST00000318445, ENST00000424469); non_coding_transcript_exon_variant(ENST00000553653, ENST00000555549, ENST00000555769, ENST00000556649); non_coding_transcript_variant(ENST00000553653, ENST00000555549, ENST00000555769, ENST00000556649)
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)
SLCO3A1	solute carrier organic anion transporter family, member 3A1	15q26	2(1/1/0)

SNPs in LD with rs1517618 (count: 0) View in gBrowse (chr15:92104415..92104415 )

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

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