SNP Report

Basic Info

Name	rs4475032 dbSNP Ensembl
Location	chr3:52526005 - 52526005(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.332069
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000321725, ENST00000462681, ENST00000462741, ENST00000469989, ENST00000471522, ENST00000481626, ENST00000486792, ENST00000487779, ENST00000489316, ENST00000490681); intron_variant(ENST00000307076, ENST00000422318, ENST00000459839, ENST00000463947, ENST00000466112, ENST00000478091, ENST00000492555); NMD_transcript_variant(ENST00000492555); non_coding_transcript_exon_variant(ENST00000462261, ENST00000479024); non_coding_transcript_variant(ENST00000462261, ENST00000466112, ENST00000478091, ENST00000479024); upstream_gene_variant(ENST00000469616)
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)
STAB1	stabilin 1	3p21.31	Mapped by Literature SNP
NT5DC2	5'-nucleotidase domain containing 2	3p21.1	Mapped by LD-proxy

SNPs in LD with rs4475032 (count: 0) View in gBrowse (chr3:52526005..52526005 )

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

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