SNP Report

Basic Info

Name	rs4733788 dbSNP Ensembl
Location	chr8:130324790 - 130324790(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.220048
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000357668, ENST00000518721, ENST00000520927, ENST00000521075, ENST00000521426, ENST00000524299, ENST00000524367); NMD_transcript_variant(ENST00000520927, ENST00000521075, ENST00000524299); non_coding_transcript_variant(ENST00000524367)
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)
ASAP1	ArfGAP with SH3 domain, ankyrin repeat and PH domain 1	8q24.1-q24.2	1(0/1/0)

SNPs in LD with rs4733788 (count: 0) View in gBrowse (chr8:130324790..130324790 )

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

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