PTSDgene database

SNP Report

Basic Info
Name rs17054232 dbSNP Ensembl
Location 4:168475606 - 168475606(+)
Variant Seq A
Ancestral Allele G
Ref Seq G
Minor Allele Frequence 0.343251
Annotation downstream_gene_variant; intron_variant; non_coding_transcript_variant
Variant Effect downstream_gene_variant(ENST00000384442, ENST00000505150); intron_variant(ENST00000513901, ENST00000505696, ENST00000511577, ENST00000512371, ENST00000260184, ENST00000514748, ENST00000505890, ENST00000515088); non_coding_transcript_variant(ENST00000513901, ENST00000515088)
SIFT Annotation deleterious
SIFT Variant Effect deleterious(ENST00000505890, ENST00000260184, ENST00000511577, ENST00000514748, ENST00000512371, ENST00000505696)
PolyPhen Annotation possibly_damaging
PolyPhen Variant Effect possibly_damaging(ENST00000505890, ENST00000260184, ENST00000511577, ENST00000514748, ENST00000512371, ENST00000505696)
rSNP? Yes Link in rVarBase
Related Regulatory Elements Chromatin interactive region
Chromatin State Enhancers;Weak transcription;Genic 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)
DDX60L DEAD-box helicase 60-like 4q32.3 1(0/0/1)

SNPs in LD with rs17054232 (count: 0)

SNP related eQTL (count: 1)
Gene Symbol Gene Existed in PTSDgene? Tissue Trans/Cis Source
CRHR1-IT1 Yes Adipose Subcutaneous cis GTEx