SNP Report

Basic Info

Name	rs4901075 dbSNP Ensembl
Location	chr14:51056701 - 51056701(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.260982
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000298355, ENST00000338969, ENST00000360392)
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)
TRIM9	tripartite motif containing 9	14q21.3	1(0/1/0)

SNPs in LD with rs4901075 (count: 0) View in gBrowse (chr14:51056701..51056701 )

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

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