PTSDgene database

SNP Report

Basic Info
Name rs4713899 dbSNP Ensembl
Location 6:35601504 - 35601504(+)
Variant Seq G
Ancestral Allele G
Ref Seq A
Minor Allele Frequence 0.164137
Annotation intron_variant
Variant Effect intron_variant(ENST00000542713, ENST00000539068, ENST00000357266, ENST00000536438)
SIFT Annotation tolerated
SIFT Variant Effect tolerated(ENST00000357266, ENST00000539068, ENST00000536438)
PolyPhen Annotation benign
PolyPhen Variant Effect benign(ENST00000357266, ENST00000539068, ENST00000536438)
rSNP? Yes Link in rVarBase
Related Regulatory Elements Chromatin interactive region
Chromatin State Enhancers;Weak transcription;Flanking Active TSS;Active TSS;Bivalent Enhancer
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)
ARMC12 armadillo repeat containing 12 6p21.31 rSNP target
FKBP5 FK506 binding protein 5 6p21.31 25(12/13/0)

SNPs in LD with rs4713899 (count: 0)

SNP related eQTL (count: 1)
Gene Symbol Gene Existed in PTSDgene? Tissue Trans/Cis Source
CRHR1 Yes Adipose Subcutaneous cis GTEx