SNP Report

Basic Info

Name	rs4786120 dbSNP Ensembl
Location	chr16:6753551 - 6753551(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.169928
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000516271); intron_variant(ENST00000422070, ENST00000535565, ENST00000547372, ENST00000547427, ENST00000547605, ENST00000550418, ENST00000551752, ENST00000552089, ENST00000553186, ENST00000569895); non_coding_transcript_variant(ENST00000547427, ENST00000569895)
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)
RBFOX1	RNA binding protein, fox-1 homolog (C. elegans) 1	16p13.3	6(2/2/2)
RNU7-99P	RNA, U7 small nuclear 99 pseudogene	16p13.3	Mapped by Literature SNP

SNPs in LD with rs4786120 (count: 0) View in gBrowse (chr16:6753551..6753551 )

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

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