SNP Report

Basic Info

Name	rs12889168 dbSNP Ensembl
Location	chr14:104015620 - 104015620(1)
Variant Alleles	A/T
Ancestral Allele	A
Minor Allele	T
Minor Allele Frequence	0.264776
Functional Annotation	downstream_gene_variant; intron_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000485467); intron_variant(ENST00000339063, ENST00000409874, ENST00000557332)
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)
RN7SL634P	RNA, 7SL, cytoplasmic 634, pseudogene	14q32.33	Mapped by LD-proxy
TDRD9	tudor domain containing 9	14q32.33	3(1/1/1)

SNPs in LD with rs12889168 (count: 0) View in gBrowse (chr14:104015620..104015620 )

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

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