PTSDgene database

SNP Report

Basic Info
Name rs1876827 dbSNP Ensembl
Location 17:45834466 - 45834466(+)
Variant Seq C
Ancestral Allele C
Ref Seq T
Minor Allele Frequence 0.0860623
Annotation downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant
Variant Effect downstream_gene_variant(ENST00000582766, ENST00000581479, ENST00000580955); intron_variant(ENST00000634540, ENST00000634876, ENST00000347197, ENST00000398285, ENST00000583888, ENST00000619154, ENST00000314537, ENST00000580876, ENST00000339069, ENST00000293493, ENST00000535778, ENST00000352855, ENST00000577353); NMD_transcript_variant(ENST00000347197, ENST00000583888, ENST00000535778); non_coding_transcript_variant(ENST00000634876)
SIFT Annotation deleterious; tolerated
SIFT Variant Effect deleterious(ENST00000314537, ENST00000293493, ENST00000398285, ENST00000352855); tolerated(ENST00000577353, ENST00000339069, ENST00000634540)
PolyPhen Annotation benign; probably_damaging; possibly_damaging
PolyPhen Variant Effect benign(ENST00000339069); probably_damaging(ENST00000314537); possibly_damaging(ENST00000577353, ENST00000293493, ENST00000398285, ENST00000352855, ENST00000634540)
rSNP? Yes Link in rVarBase
Related Regulatory Elements n/a
Chromatin State Enhancers;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 rs1876827 (count: 0)

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