SNP Report

Basic Info

Name	rs11038689 dbSNP Ensembl
Location	chr11:45852713 - 45852713(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.153954
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000417225, ENST00000443527, ENST00000473199, ENST00000496571, ENST00000532390, ENST00000616080, ENST00000616623); non_coding_transcript_variant(ENST00000473199, ENST00000496571, ENST00000532390)
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 rs11038689 (count: 0) View in gBrowse (chr11:45852713..45852713 )

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

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