PTSDgene database

SNP Report

Basic Info
Name rs3810595 dbSNP Ensembl
Location 22:19962121 - 19962121(+)
Variant Seq C
Ancestral Allele C
Ref Seq G
Minor Allele Frequence 0.356629
Annotation upstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant
Variant Effect upstream_gene_variant(ENST00000428707, ENST00000493893, ENST00000585066, ENST00000449653); intron_variant(ENST00000406520, ENST00000207636, ENST00000403710, ENST00000403184, ENST00000361682, ENST00000407537, ENST00000467943, ENST00000412786); NMD_transcript_variant(ENST00000207636); non_coding_transcript_variant(ENST00000467943)
SIFT Annotation tolerated
SIFT Variant Effect tolerated(ENST00000406520, ENST00000412786, ENST00000361682, ENST00000207636, ENST00000407537, ENST00000449653, ENST00000403184, ENST00000403710)
PolyPhen Annotation benign
PolyPhen Variant Effect benign(ENST00000406520, ENST00000412786, ENST00000361682, ENST00000207636, ENST00000407537, ENST00000449653, ENST00000403184, ENST00000403710)
rSNP? No Link in rVarBase
Related Regulatory Elements N.A.
Chromatin State N.A.
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)
COMT catechol-O-methyltransferase 22q11.21 21(9/12/0)

SNPs in LD with rs3810595 (count: 0)

SNP related eQTL (count: 1)
Gene Symbol Gene Existed in PTSDgene? Tissue Trans/Cis Source
FBLL1 No Adipose Subcutaneous cis GTEx