PTSDgene database

SNP Report

Basic Info
Name rs11606304 dbSNP Ensembl
Location 11:18030701 - 18030701(+)
Variant Seq G
Ancestral Allele T
Ref Seq T
Minor Allele Frequence 0.0283546
Annotation intron_variant; NMD_transcript_variant
Variant Effect intron_variant(ENST00000417164, ENST00000528338, ENST00000250018); NMD_transcript_variant(ENST00000417164)
SIFT Annotation deleterious
SIFT Variant Effect deleterious(ENST00000250018)
PolyPhen Annotation probably_damaging
PolyPhen Variant Effect probably_damaging(ENST00000250018)
rSNP? Yes Link in rVarBase
Related Regulatory Elements n/a
Chromatin State Weak transcription
No. of Marker's Association Results 2 (Positive: 0; Negative: 2; Trend: 0)
Source Literature

SNP related association results
Normal genetic study related association results (count: 2)
Reference Phenotype Statistical Values Author Comments Marker's Category
Solovieff, N.,2014 PTSD diagnosis P-value=0.077 P-value=0.077 Achieved nominal levels of significance with PTSD diagnosis,...... Achieved nominal levels of significance with PTSD diagnosis, although was not significant after correction for multiple testing More... Non-significant
Solovieff, N.,2014 PTSD severity P-value=0.120 P-value=0.120 Achieved nominal levels of significance with PTSD severity, ...... Achieved nominal levels of significance with PTSD severity, although was not significant after correction for multiple testing More... Non-significant


SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Association Results (Positive/Negative/Trend)
TPH1 tryptophan hydroxylase 1 11p15.3-p14 5(1/4/0)

SNPs in LD with rs11606304 (count: 0)

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