PTSDgene database

SNP Report

Basic Info
Name rs17689882 dbSNP Ensembl
Location 17:45829462 - 45829462(+)
Variant Seq A
Ancestral Allele G
Ref Seq G
Minor Allele Frequence 0.086262
Annotation upstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant
Variant Effect upstream_gene_variant(ENST00000580876, ENST00000535778, ENST00000581479); intron_variant(ENST00000352855, ENST00000582766, ENST00000339069, ENST00000634540, ENST00000634876, ENST00000398285, ENST00000314537, ENST00000580955, ENST00000293493, ENST00000577353, ENST00000619154, ENST00000583888, ENST00000347197); NMD_transcript_variant(ENST00000580955, ENST00000583888, ENST00000347197); non_coding_transcript_variant(ENST00000582766, ENST00000634876)
SIFT Annotation deleterious_-_low_confidence; tolerated
SIFT Variant Effect deleterious_-_low_confidence(ENST00000619154); tolerated(ENST00000293493, ENST00000314537, ENST00000352855, ENST00000583888, ENST00000398285, ENST00000339069, ENST00000577353)
PolyPhen Annotation unknown; benign
PolyPhen Variant Effect unknown(ENST00000619154); benign(ENST00000293493, ENST00000314537, ENST00000352855, ENST00000583888, ENST00000398285, ENST00000339069, ENST00000577353)
rSNP? Yes Link in rVarBase
Related Regulatory Elements TF binding region
Chromatin State Strong transcription;Bivalent Enhancer;Weak transcription
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)
CRHR1 corticotropin releasing hormone receptor 1 17q21.31 12(6/6/0)
MAPT-AS1 MAPT antisense RNA 1 17q21.31 Mapped by Literature SNP, Mapped by LD-proxy, rSNP target

SNPs in LD with rs17689882 (count: 0)

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