SNP Report

Basic Info

Name	rs9819038 dbSNP Ensembl
Location	chr3:193605081 - 193605081(1)
Variant Alleles	T/G
Ancestral Allele	T
Minor Allele	G
Minor Allele Frequence	0.392372
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000361150, ENST00000361510, ENST00000361715, ENST00000361828, ENST00000361908, ENST00000392436, ENST00000392437, ENST00000392438, ENST00000419435, LRG_337t1, LRG_337t2)
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)
OPA1	optic atrophy 1 (autosomal dominant)	3q29	1(0/1/0)

SNPs in LD with rs9819038 (count: 0) View in gBrowse (chr3:193605081..193605081 )

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

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