SNP Report

Basic Info

Name	rs11038914 dbSNP Ensembl
Location	chr11:46539751 - 46539751(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.245407
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000314845, ENST00000458649, ENST00000528950, ENST00000533727, ENST00000534300)
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)
AMBRA1	autophagy/beclin-1 regulator 1	11p11.2	Mapped by LD-proxy

SNPs in LD with rs11038914 (count: 0) View in gBrowse (chr11:46539751..46539751 )

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

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