SNP Report

Basic Info

Name	rs3824755 dbSNP Ensembl
Location	chr10:102836092 - 102836092(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.21865
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000369884, ENST00000445829); intron_variant(ENST00000369887, ENST00000489268); non_coding_transcript_variant(ENST00000489268); upstream_gene_variant(ENST00000469683)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 3)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
PFN1P11	profilin 1 pseudogene 11	10q24.32	Mapped by LD-proxy
CYP17A1	cytochrome P450, family 17, subfamily A, polypeptide 1	10q24.3	Mapped by LD-proxy
CYP17A1-AS1	CYP17A1 antisense RNA 1	10q24.32	Mapped by LD-proxy

SNPs in LD with rs3824755 (count: 0) View in gBrowse (chr10:102836092..102836092 )

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

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