SNP Report

Basic Info

Name	rs2292912 dbSNP Ensembl
Location	chr11:45856137 - 45856137(1)
Variant Alleles	C/G/T
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.499601
Functional Annotation	intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000417225, ENST00000443527, ENST00000473199, ENST00000532390, ENST00000616080, ENST00000616623); non_coding_transcript_exon_variant(ENST00000496571); non_coding_transcript_variant(ENST00000473199, ENST00000496571, ENST00000532390); upstream_gene_variant(ENST00000525110, ENST00000533779)
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)
CRY2	cryptochrome circadian clock 2	11p11.2	5(3/2/0)

SNPs in LD with rs2292912 (count: 0) View in gBrowse (chr11:45856137..45856137 )

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

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