SNP Report

Basic Info

Name	rs228727 dbSNP Ensembl
Location	chr1:7787776 - 7787776(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.463259
Functional Annotation	intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000361923, ENST00000377532, ENST00000377541, ENST00000473653, ENST00000613533, ENST00000614998); non_coding_transcript_exon_variant(ENST00000602883); non_coding_transcript_variant(ENST00000473653, ENST00000602883)
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 rs228727 (count: 0) View in gBrowse (chr1:7787776..7787776 )

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

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