SNP Report

Basic Info
Name rs1364565 dbSNP Ensembl
Location chr2:107530006 - 107530006(1)
Variant Alleles A/G
Ancestral Allele G
Minor Allele A
Minor Allele Frequence 0.293331
Functional Annotation intron_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000414300, ENST00000443205); non_coding_transcript_variant(ENST00000414300, ENST00000443205)
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 rs1364565 (count: 0) View in gBrowse (chr2:107530006..107530006 )

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

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