SNP Report

Basic Info

Name	rs4849301 dbSNP Ensembl
Location	chr2:110965891 - 110965891(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.336861
Functional Annotation	intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000389811, ENST00000417074, ENST00000433706, ENST00000439055, ENST00000443586); NMD_transcript_variant(ENST00000443586); upstream_gene_variant(ENST00000448118)
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)
ACOXL	acyl-CoA oxidase-like	2q13	2(0/2/0)
RPL5P9	ribosomal protein L5 pseudogene 9	2q13	Mapped by Literature SNP

SNPs in LD with rs4849301 (count: 0) View in gBrowse (chr2:110965891..110965891 )

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

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