SNP Report

Basic Info

Name	rs2028264 dbSNP Ensembl
Location	chr16:19556775 - 19556775(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.121605
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000381396, ENST00000396208, ENST00000396212); intron_variant(ENST00000251143, ENST00000417362, ENST00000438132, ENST00000513947, ENST00000537186, ENST00000539322, ENST00000542263, ENST00000543460, ENST00000544670, ENST00000567245); NMD_transcript_variant(ENST00000537186, ENST00000539322); non_coding_transcript_variant(ENST00000543460)
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)
C16orf62	chromosome 16 open reading frame 62	16p12.3	Mapped by LD-proxy
CCP110	centriolar coiled coil protein 110kDa	16p12.3	1(0/0/1)

SNPs in LD with rs2028264 (count: 0) View in gBrowse (chr16:19556775..19556775 )

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

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