SNP Report

Basic Info

Name	rs4733569 dbSNP Ensembl
Location	chr8:130086991 - 130086991(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.214058
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000357668, ENST00000518721, ENST00000519483, ENST00000520189, ENST00000521075, ENST00000524124); NMD_transcript_variant(ENST00000521075); non_coding_transcript_variant(ENST00000520189); upstream_gene_variant(ENST00000626977)
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 rs4733569 (count: 0) View in gBrowse (chr8:130086991..130086991 )

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

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