PTSDgene database

SNP Report

Basic Info
Name rs685247 dbSNP Ensembl
Location 11:18039039 - 18039039(+)
Variant Seq T
Ancestral Allele C
Ref Seq C
Minor Allele Frequence 0.305112
Annotation intron_variant; NMD_transcript_variant
Variant Effect intron_variant(ENST00000417164, ENST00000250018, ENST00000528338); NMD_transcript_variant(ENST00000417164)
SIFT Annotation deleterious
SIFT Variant Effect deleterious(ENST00000417164, ENST00000528338, ENST00000250018)
PolyPhen Annotation probably_damaging
PolyPhen Variant Effect probably_damaging(ENST00000417164, ENST00000528338, ENST00000250018)
rSNP? No Link in rVarBase
Related Regulatory Elements n/a
Chromatin State Inactive region
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)
TPH1 tryptophan hydroxylase 1 11p15.3-p14 5(1/4/0)

SNPs in LD with rs685247 (count: 0)

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