SNP Report

Basic Info

Name	rs2066612 dbSNP Ensembl
Location	chr13:50171259 - 50171259(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.343051
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000461527, ENST00000463474, ENST00000467721, ENST00000468168, ENST00000468522, ENST00000476738, ENST00000486895, ENST00000490577, ENST00000491341, ENST00000491615); non_coding_transcript_variant(ENST00000461527, ENST00000463474, ENST00000467721, ENST00000468168, ENST00000468522, ENST00000476738, ENST00000486895, ENST00000490577, ENST00000491341, ENST00000491615); upstream_gene_variant(ENST00000495613)
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)
ST13P4	suppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 4	13q14	Mapped by Literature SNP
DLEU1	deleted in lymphocytic leukemia 1 (non-protein coding)	13q14.3	Mapped by Literature SNP

SNPs in LD with rs2066612 (count: 0) View in gBrowse (chr13:50171259..50171259 )

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

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