SNP Report

Basic Info

Name	rs8176914 dbSNP Ensembl
Location	chr12:79590919 - 79590919(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.260982
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000328827); downstream_gene_variant(ENST00000547699); intron_variant(ENST00000548075, ENST00000549050, ENST00000550603); non_coding_transcript_variant(ENST00000548075, ENST00000549050)
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 rs8176914 (count: 0) View in gBrowse (chr12:79590919..79590919 )

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

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