PTSDgene database

SNP Report

Basic Info
Name rs1076153 dbSNP Ensembl
Location 9:133633021 - 133633021(+)
Variant Seq T
Ancestral Allele G
Ref Seq G
Minor Allele Frequence 0.352835
Annotation non_coding_transcript_exon_variant; upstream_gene_variant; non_coding_transcript_variant
Variant Effect non_coding_transcript_exon_variant(ENST00000564021); upstream_gene_variant(ENST00000263611, ENST00000393056); non_coding_transcript_variant(ENST00000564021)
SIFT Annotation deleterious
SIFT Variant Effect deleterious(ENST00000356873, ENST00000496132)
PolyPhen Annotation possibly_damaging
PolyPhen Variant Effect possibly_damaging(ENST00000356873, ENST00000496132)
rSNP? Yes Link in rVarBase
Related Regulatory Elements TF binding region;lncRNA
Chromatin State Enhancers;Weak transcription;Bivalent Enhancer
No. of Marker's Association Results 1 (Positive: 0; Negative: 1; Trend: 0)
Source Literature

SNP related association results
Normal genetic study related association results (count: 1)
Reference Phenotype Statistical Values Author Comments Marker's Category
Solovieff, N.,2014 PTSD severity P-value=0.154 P-value=0.154 Achieved nominal levels of significance with PTSD severity, ...... Achieved nominal levels of significance with PTSD severity, although was not significant after correction for multiple testing More... Non-significant


SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Association Results (Positive/Negative/Trend)
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase) 9q34 4(0/4/0)

SNPs in LD with rs1076153 (count: 2)
The LD data used here is based on 1000 Genome Phase I. LD SNP pairs were selected with a threshold r2<=0.8.

Literature-origin SNPs (count: 0)

LD-proxies (count: 2)


SNP related eQTL (count: 1)
Gene Symbol Gene Existed in PTSDgene? Tissue Trans/Cis Source
RP11-707O23.5 No Adipose Subcutaneous cis GTEx