SNP Report

Basic Info

Name	rs7662693 dbSNP Ensembl
Location	chr4:52617076 - 52617076(1)
Variant Alleles	C/G
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.157348
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000441222, ENST00000451218, ENST00000503060, ENST00000508499, ENST00000514536); NMD_transcript_variant(ENST00000503060, ENST00000514536)
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)
USP46	ubiquitin specific peptidase 46	4q12	1(0/1/0)

SNPs in LD with rs7662693 (count: 0) View in gBrowse (chr4:52617076..52617076 )

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

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