SNP Report

Basic Info

Name	rs10014556 dbSNP Ensembl
Location	chr4:52657558 - 52657558(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.19389
Functional Annotation	intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000441222, ENST00000451218, ENST00000503060, ENST00000514536); NMD_transcript_variant(ENST00000503060, ENST00000514536); upstream_gene_variant(ENST00000503051, ENST00000504078, ENST00000506707, ENST00000508499, ENST00000512656)
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)
USP46-AS1	USP46 antisense RNA 1	4q12	Mapped by LD-proxy
USP46	ubiquitin specific peptidase 46	4q12	1(0/1/0)

SNPs in LD with rs10014556 (count: 0) View in gBrowse (chr4:52657558..52657558 )

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

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