SNP Report

Basic Info

Name	rs2738889 dbSNP Ensembl
Location	chr1:181781965 - 181781965(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.288938
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000357570, ENST00000358338, ENST00000360108, ENST00000367567, ENST00000367570, ENST00000367573, ENST00000621551, ENST00000621791)
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)
CACNA1E	calcium channel, voltage-dependent, R type, alpha 1E subunit	1q25.3	1(1/0/0)

SNPs in LD with rs2738889 (count: 0) View in gBrowse (chr1:181781965..181781965 )

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

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