SNP Report

Basic Info

Name	rs3783855 dbSNP Ensembl
Location	chr14:89332044 - 89332044(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.152556
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000261302, ENST00000345097, ENST00000553353, ENST00000553840, ENST00000554005, ENST00000555353, ENST00000555658, ENST00000556916, ENST00000557258, ENST00000557718, ENST00000615335); NMD_transcript_variant(ENST00000554005, ENST00000557718); non_coding_transcript_variant(ENST00000555658)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
FOXN3	forkhead box N3	14q32.11	1(1/0/0)

SNPs in LD with rs3783855 (count: 0) View in gBrowse (chr14:89332044..89332044 )

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

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