PTSDgene database

SNP Report

Basic Info
Name rs564585 dbSNP Ensembl
Location 15:78593885 - 78593885(+)
Variant Seq G
Ancestral Allele A
Ref Seq A
Minor Allele Frequence 0.444489
Annotation downstream_gene_variant; upstream_gene_variant; 3_prime_UTR_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant
Variant Effect downstream_gene_variant(ENST00000559576, ENST00000326828, ENST00000394802, ENST00000559554); upstream_gene_variant(ENST00000567141); 3_prime_UTR_variant(ENST00000299565); intron_variant(ENST00000348639, ENST00000559002, ENST00000559658); NMD_transcript_variant(ENST00000559658); non_coding_transcript_variant(ENST00000559002)
SIFT Annotation tolerated
SIFT Variant Effect tolerated(ENST00000326828, ENST00000559658, ENST00000348639)
PolyPhen Annotation benign
PolyPhen Variant Effect benign(ENST00000326828, ENST00000559658, ENST00000348639)
rSNP? Yes Link in rVarBase
Related Regulatory Elements n/a
Chromatin State Weak transcription;Strong transcription
No. of Marker's Association Results 0 (Positive: 0; Negative: 0; Trend: 0)
Source LD-proxy

SNP related association results


SNP related genes (count: 2)
Approved Symbol Approved Name Location No. of Association Results (Positive/Negative/Trend)
CHRNA3 cholinergic receptor, nicotinic alpha 3 15q24 1(0/1/0)
CHRNA5 cholinergic receptor, nicotinic alpha 5 15q24 2(1/1/0)

SNPs in LD with rs564585 (count: 0)

SNP related eQTL (count: 1)
Gene Symbol Gene Existed in PTSDgene? Tissue Trans/Cis Source
RP11-259G18.3 No Adipose Subcutaneous cis GTEx