PTSDgene database

SNP Report

Basic Info
Name rs10241138 dbSNP Ensembl
Location 7:31056747 - 31056747(+)
Variant Seq C
Ancestral Allele T
Ref Seq T
Minor Allele Frequence 0.185903
Annotation upstream_gene_variant; intron_variant
Variant Effect upstream_gene_variant(ENST00000431811); intron_variant(ENST00000409363, ENST00000304166, ENST00000614107)
SIFT Annotation deleterious
SIFT Variant Effect deleterious(ENST00000326139, ENST00000409904)
PolyPhen Annotation benign
PolyPhen Variant Effect benign(ENST00000326139, ENST00000409904)
rSNP? Yes Link in rVarBase
Related Regulatory Elements TF binding region;Chromatin interactive region
Chromatin State Enhancers;Weak transcription;Active TSS;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
Ressler, K. J.,2011 PTSD diagnosis Females: P-value=0.948, males: P-value=0.883 Females: P-value=0.948, males: P-value=0.883 No significant result in females or males after multiple cor...... No significant result in females or males after multiple corrections. More... Non-significant


SNP related genes (count: 2)
Approved Symbol Approved Name Location No. of Association Results (Positive/Negative/Trend)
GHRHR growth hormone releasing hormone receptor 7p14 rSNP target
ADCYAP1R1 adenylate cyclase activating polypeptide 1 (pituitary) receptor type I 7p14.3 19(8/11/0)

SNPs in LD with rs10241138 (count: 0)

SNP related eQTL (count: 1)
Gene Symbol Gene Existed in PTSDgene? Tissue Trans/Cis Source
LRRC37A4P No Adipose Subcutaneous cis GTEx