SNP Report

Basic Info
Name rs7953683 dbSNP Ensembl
Location chr12:79599924 - 79599924(1)
Variant Alleles C/T
Ancestral Allele C
Minor Allele T
Minor Allele Frequence 0.259585
Functional Annotation downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000551712); intron_variant(ENST00000328827, ENST00000549050); non_coding_transcript_variant(ENST00000549050); upstream_gene_variant(ENST00000547699, ENST00000548075, ENST00000550603)
No. of Studies 0 (Positive: 0; Negative: 0; Trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
PAWR PRKC, apoptosis, WT1, regulator 12q21.2 1(0/1/0)

SNPs in LD with rs7953683 (count: 0) View in gBrowse (chr12:79599924..79599924 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)