PTSDgene database

SNP Report

Basic Info
Name rs3919455 dbSNP Ensembl
Location 17:45876341 - 45876341(+)
Variant Seq T
Ancestral Allele T
Ref Seq C
Minor Allele Frequence 0.0860623
Annotation intron_variant; non_coding_transcript_variant
Variant Effect intron_variant(ENST00000634876, ENST00000579599, ENST00000579244); non_coding_transcript_variant(ENST00000634876, ENST00000579599, ENST00000579244)
SIFT Annotation tolerated
SIFT Variant Effect tolerated(ENST00000329196)
PolyPhen Annotation benign
PolyPhen Variant Effect benign(ENST00000329196)
rSNP? Yes Link in rVarBase
Related Regulatory Elements n/a
Chromatin State 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: 1)
Approved Symbol Approved Name Location No. of Association Results (Positive/Negative/Trend)
MAPT-AS1 MAPT antisense RNA 1 17q21.31 Mapped by Literature SNP, Mapped by LD-proxy, rSNP target

SNPs in LD with rs3919455 (count: 0)

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