PTSDgene database

SNP Report

Basic Info
Name rs11072768 dbSNP Ensembl
Location 15:78637136 - 78637136(+)
Variant Seq G
Ancestral Allele T
Ref Seq T
Minor Allele Frequence 0.445687
Annotation intron_variant; NMD_transcript_variant; non_coding_transcript_variant
Variant Effect intron_variant(ENST00000261751, ENST00000559849, ENST00000560511, ENST00000412074); NMD_transcript_variant(ENST00000559849); non_coding_transcript_variant(ENST00000560511)
SIFT Annotation tolerated_-_low_confidence; tolerated
SIFT Variant Effect tolerated_-_low_confidence(ENST00000412074); tolerated(ENST00000261751)
PolyPhen Annotation benign
PolyPhen Variant Effect benign(ENST00000261751, ENST00000412074)
rSNP? Yes Link in rVarBase
Related Regulatory Elements Chromatin interactive region
Chromatin State Weak transcription;Enhancers
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)
QRICH1 glutamine-rich 1 3p21.31 rSNP target
CHRNB4 cholinergic receptor, nicotinic beta 4 15q24 Mapped by Literature SNP, Mapped by LD-proxy, rSNP target

SNPs in LD with rs11072768 (count: 0)

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