SNP Report

Basic Info

Name	rs16904197 dbSNP Ensembl
Location	chr8:130064019 - 130064019(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.215655
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000357668, ENST00000518721, ENST00000519483, ENST00000521075, ENST00000524124); NMD_transcript_variant(ENST00000521075)
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 rs16904197 (count: 0) View in gBrowse (chr8:130064019..130064019 )

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

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