SNP Report

Basic Info

Name	rs2503712 dbSNP Ensembl
Location	chr1:2205929 - 2205929(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.486821
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000469733, ENST00000487186); non_coding_transcript_variant(ENST00000469733, ENST00000487186); upstream_gene_variant(ENST00000514625)
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)
C1orf86	chromosome 1 open reading frame 86	1p36.33	Mapped by Literature SNP

SNPs in LD with rs2503712 (count: 0) View in gBrowse (chr1:2205929..2205929 )

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

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