PTSDgene database

SNP Report

Basic Info
Name rs8078900 dbSNP Ensembl
Location 17:30264691 - 30264691(+)
Variant Seq A
Ancestral Allele C
Ref Seq C
Minor Allele Frequence 0.252196
Annotation downstream_gene_variant; intron_variant; NMD_transcript_variant
Variant Effect downstream_gene_variant(ENST00000579957, ENST00000577623); intron_variant(ENST00000261714, ENST00000578090); NMD_transcript_variant(ENST00000578090)
SIFT Annotation tolerated
SIFT Variant Effect tolerated(ENST00000261714)
PolyPhen Annotation probably_damaging
PolyPhen Variant Effect probably_damaging(ENST00000261714)
rSNP? Yes Link in rVarBase
Related Regulatory Elements Chromatin interactive region
Chromatin State Weak transcription;Strong transcription;Active TSS;Genic enhancers;Enhancers;Flanking Active TSS
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)
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4 17q11.2 44(13/31/0)
BLMH bleomycin hydrolase 17q11.2 Mapped by LD-proxy

SNPs in LD with rs8078900 (count: 0)

SNP related eQTL (count: 1)
Gene Symbol Gene Existed in PTSDgene? Tissue Trans/Cis Source
DND1P1 No Adipose Subcutaneous cis GTEx