SNP Report

Basic Info

Name	rs774047 dbSNP Ensembl
Location	chr12:56422138 - 56422138(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.498802
Functional Annotation	missense_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant. Polyphen Annotation: benign(ENST00000229201, ENST00000553532) SIFT Annotation: tolerated(ENST00000229201, ENST00000553532)
Consequence to Transcript	missense_variant(ENST00000229201, ENST00000553532); non_coding_transcript_exon_variant(ENST00000555808, ENST00000557589); non_coding_transcript_variant(ENST00000555808, ENST00000557589); upstream_gene_variant(ENST00000553314)
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)
TIMELESS	timeless circadian clock	12q13.3	3(0/3/0)

SNPs in LD with rs774047 (count: 0) View in gBrowse (chr12:56422138..56422138 )

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

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