SNP Report

Basic Info

Name	rs6770913 dbSNP Ensembl
Location	chr3:193620546 - 193620546(1)
Variant Alleles	C/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.467652
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000392437, ENST00000419435); intron_variant(ENST00000361150, ENST00000361510, ENST00000361715, ENST00000361828, ENST00000361908, ENST00000392436, ENST00000392438, ENST00000433105, ENST00000434811, ENST00000444085, ENST00000487986, ENST00000497189, LRG_337t1, LRG_337t2); non_coding_transcript_variant(ENST00000433105, ENST00000444085, ENST00000487986, ENST00000497189); upstream_gene_variant(ENST00000384640)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
OPA1	optic atrophy 1 (autosomal dominant)	3q29	1(0/1/0)
OPA1-AS1	OPA1 antisense RNA 1	3q29	Mapped by Literature SNP

SNPs in LD with rs6770913 (count: 0) View in gBrowse (chr3:193620546..193620546 )

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

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