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)