SNP Report

Basic Info

Name	rs1420378 dbSNP Ensembl
Location	chr2:170774121 - 170774121(1)
Variant Alleles	C/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.223442
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000426475, ENST00000429172); non_coding_transcript_variant(ENST00000426475, ENST00000429172); upstream_gene_variant(ENST00000442456, ENST00000623867)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 0)

SNPs in LD with rs1420378 (count: 0) View in gBrowse (chr2:170774121..170774121 )

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

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