SNP Report

Basic Info

Name	rs4908694 dbSNP Ensembl
Location	chr1:7790838 - 7790838(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.0922524
Functional Annotation	downstream_gene_variant; intron_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000473653, ENST00000602883); intron_variant(ENST00000361923, ENST00000377532, ENST00000377541, ENST00000613533, ENST00000614998)
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)
PER3	period circadian clock 3	1p36.23	7(3/4/0)

SNPs in LD with rs4908694 (count: 0) View in gBrowse (chr1:7790838..7790838 )

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

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