SNP Report

Basic Info

Name	rs4765815 dbSNP Ensembl
Location	chr12:5455743 - 5455743(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.0980431
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000423158, ENST00000535299, ENST00000543548); non_coding_transcript_variant(ENST00000535299, ENST00000543548)
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)
NTF3	neurotrophin 3	12p13	Mapped by Literature SNP

SNPs in LD with rs4765815 (count: 0) View in gBrowse (chr12:5455743..5455743 )

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

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