SNP Report

Basic Info
Name rs8176805 dbSNP Ensembl
Location chr12:79690012 - 79690012(1)
Variant Alleles G/C
Ancestral Allele G
Minor Allele C
Minor Allele Frequence 0.258187
Functional Annotation downstream_gene_variant; missense_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Polyphen Annotation: unknown(ENST00000551712); benign(ENST00000328827)
SIFT Annotation: tolerated - low confidence(ENST00000551712); deleterious(ENST00000328827)
Consequence to Transcript downstream_gene_variant(ENST00000548426, ENST00000552637); missense_variant(ENST00000328827, ENST00000551712); non_coding_transcript_exon_variant(ENST00000547016, ENST00000547571, ENST00000550006); non_coding_transcript_variant(ENST00000547016, ENST00000547571, ENST00000550006); upstream_gene_variant(ENST00000551995)
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 rs8176805 (count: 0) View in gBrowse (chr12:79690012..79690012 )

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

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