PTSDgene database

SNP Report

Basic Info
Name rs10040267 dbSNP Ensembl
Location 5:168461626 - 168461626(+)
Variant Seq A
Ancestral Allele G
Ref Seq G
Minor Allele Frequence 0.259784
Annotation upstream_gene_variant; intron_variant; non_coding_transcript_variant
Variant Effect upstream_gene_variant(ENST00000521391); intron_variant(ENST00000521089, ENST00000265293, ENST00000619752, ENST00000522140, ENST00000524228, ENST00000524038, ENST00000393895); non_coding_transcript_variant(ENST00000522140)
SIFT Annotation tolerated
SIFT Variant Effect tolerated(ENST00000524228, ENST00000521089, ENST00000393895, ENST00000619752, ENST00000524038, ENST00000265293)
PolyPhen Annotation possibly_damaging
PolyPhen Variant Effect possibly_damaging(ENST00000524228, ENST00000521089, ENST00000393895, ENST00000619752, ENST00000524038, ENST00000265293)
rSNP? Yes Link in rVarBase
Related Regulatory Elements n/a
Chromatin State Weak transcription;Strong 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: 1)
Approved Symbol Approved Name Location No. of Association Results (Positive/Negative/Trend)
WWC1 WW and C2 domain containing 1 5q34 6(6/0/0)

SNPs in LD with rs10040267 (count: 0)

SNP related eQTL (count: 1)
Gene Symbol Gene Existed in PTSDgene? Tissue Trans/Cis Source
CRHR1-IT1 Yes Adipose Subcutaneous cis GTEx