SNP Report

Basic Info

Name	rs2118906 dbSNP Ensembl
Location	chr2:111066085 - 111066085(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.0473243
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000389811, ENST00000417074, ENST00000439055, ENST00000441974, ENST00000443586); NMD_transcript_variant(ENST00000443586)
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)
ACOXL	acyl-CoA oxidase-like	2q13	2(0/2/0)

SNPs in LD with rs2118906 (count: 0) View in gBrowse (chr2:111066085..111066085 )

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

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