SNP Report

Basic Info

Name	rs10767664 dbSNP Ensembl
Location	chr11:27704439 - 27704439(1)
Variant Alleles	T/A
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.239617
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000314915, ENST00000395978, ENST00000395981, ENST00000525950, ENST00000530663, ENST00000532997); non_coding_transcript_variant(ENST00000530663); upstream_gene_variant(ENST00000356660, ENST00000395980, ENST00000395983, ENST00000395986, ENST00000418212, ENST00000420794, ENST00000438929, ENST00000530786, ENST00000530861, ENST00000533131, ENST00000533246, ENST00000584049)
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)
BDNF	brain-derived neurotrophic factor	11p14.1	37(24/12/1)

SNPs in LD with rs10767664 (count: 0) View in gBrowse (chr11:27704439..27704439 )

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

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