SNP Report

Basic Info

Name	rs1187448 dbSNP Ensembl
Location	chr14:103940290 - 103940290(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.28095
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000557640); intron_variant(ENST00000409874, ENST00000496087, ENST00000554571); non_coding_transcript_variant(ENST00000496087, ENST00000554571)
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)
RD3L	retinal degeneration 3-like	14q32.33	Mapped by LD-proxy
TDRD9	tudor domain containing 9	14q32.33	3(1/1/1)

SNPs in LD with rs1187448 (count: 0) View in gBrowse (chr14:103940290..103940290 )

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

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