SNP Report

Basic Info

Name	rs1991287 dbSNP Ensembl
Location	chr15:88141224 - 88141224(1)
Variant Alleles	C/G
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.457468
Functional Annotation	downstream_gene_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000558776); intron_variant(ENST00000317501, ENST00000355254, ENST00000357724, ENST00000360948, ENST00000394480, ENST00000540489, ENST00000542733, ENST00000557856, ENST00000558676, ENST00000559188, ENST00000626019, ENST00000629765); upstream_gene_variant(ENST00000559764)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
NTRK3	neurotrophic tyrosine kinase, receptor, type 3	15q24-q25	2(2/0/0)
MED28P6	mediator complex subunit 28 pseudogene 6	15q25.3	Mapped by Literature SNP

SNPs in LD with rs1991287 (count: 0) View in gBrowse (chr15:88141224..88141224 )

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

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