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)