SNP Report

Basic Info

Name	rs35390666 dbSNP Ensembl
Location	chr2:238284937 - 238284937(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.0884585
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000254657, ENST00000431832); upstream_gene_variant(ENST00000637634)
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)
PER2	period circadian clock 2	2q37.3	7(1/6/0)

SNPs in LD with rs35390666 (count: 0) View in gBrowse (chr2:238284937..238284937 )

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

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