SNP Report

Basic Info
Name rs4902402 dbSNP Ensembl
Location chr14:39110424 - 39110424(1)
Variant Alleles C/T
Ancestral Allele T
Minor Allele C
Minor Allele Frequence 0.0970447
Functional Annotation downstream_gene_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000556877); upstream_gene_variant(ENST00000250379, ENST00000308317, ENST00000396249, ENST00000412033, ENST00000525153, ENST00000525430, ENST00000527381, ENST00000531684, ENST00000534684, ENST00000555425)
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)
GEMIN2 gem (nuclear organelle) associated protein 2 14q21.1 1(0/1/0)
SEC23A Sec23 homolog A (S. cerevisiae) 14q21.1 Mapped by LD-proxy

SNPs in LD with rs4902402 (count: 0) View in gBrowse (chr14:39110424..39110424 )

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

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