SNP Report

Basic Info

Name	rs7663650 dbSNP Ensembl
Location	chr4:55364952 - 55364952(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.402955
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000510637, ENST00000595103, ENST00000595734, ENST00000596289, ENST00000596312, ENST00000598906, ENST00000608086, ENST00000608265, ENST00000608558, ENST00000609051, ENST00000609487, ENST00000609500, ENST00000609573, ENST00000609580, ENST00000609700, ENST00000610396, ENST00000613794, ENST00000619685, ENST00000619912); intron_variant(ENST00000264228, ENST00000433175, ENST00000505210, ENST00000514398); non_coding_transcript_variant(ENST00000433175, ENST00000514398)
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)
SRD5A3-AS1	SRD5A3 antisense RNA 1	4q12	Mapped by LD-proxy
SRD5A3	steroid 5 alpha-reductase 3	4q12	Mapped by LD-proxy

SNPs in LD with rs7663650 (count: 0) View in gBrowse (chr4:55364952..55364952 )

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

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