PTSDgene database

SNP Report

Basic Info
Name rs16940672 dbSNP Ensembl
Location 17:45830786 - 45830786(+)
Variant Seq T
Ancestral Allele C
Ref Seq C
Minor Allele Frequence 0.0860623
Annotation downstream_gene_variant; non_coding_transcript_exon_variant; upstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant
Variant Effect downstream_gene_variant(ENST00000580955); non_coding_transcript_exon_variant(ENST00000581479); upstream_gene_variant(ENST00000535778, ENST00000580876); intron_variant(ENST00000583888, ENST00000347197, ENST00000398285, ENST00000634540, ENST00000619154, ENST00000339069, ENST00000293493, ENST00000577353, ENST00000582766, ENST00000352855, ENST00000634876, ENST00000314537); NMD_transcript_variant(ENST00000583888, ENST00000347197); non_coding_transcript_variant(ENST00000582766, ENST00000581479, ENST00000634876)
SIFT Annotation deleterious; tolerated
SIFT Variant Effect deleterious(ENST00000398285, ENST00000293493, ENST00000577353, ENST00000314537, ENST00000339069); tolerated(ENST00000352855, ENST00000634540)
PolyPhen Annotation benign; possibly_damaging; probably_damaging
PolyPhen Variant Effect benign(ENST00000293493, ENST00000339069); possibly_damaging(ENST00000398285, ENST00000577353, ENST00000634540); probably_damaging(ENST00000352855, ENST00000314537)
rSNP? Yes Link in rVarBase
Related Regulatory Elements n/a
Chromatin State 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 rs16940672 (count: 0)

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