SNP Report

Basic Info

Name	rs11072868 dbSNP Ensembl
Location	chr15:34000390 - 34000390(1)
Variant Alleles	C/A
Ancestral Allele	C
Minor Allele	A
Minor Allele Frequence	0.0896565
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000306730, ENST00000383263, ENST00000560035)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
AVEN	apoptosis, caspase activation inhibitor	15q13.1	Mapped by Literature SNP
CHRM5	cholinergic receptor, muscarinic 5	15q26	1(0/1/0)

SNPs in LD with rs11072868 (count: 0) View in gBrowse (chr15:34000390..34000390 )

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

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