SNP Report

Basic Info
Name rs11157046 dbSNP Ensembl
Location chr14:39129763 - 39129763(1)
Variant Alleles C/T
Ancestral Allele T
Minor Allele C
Minor Allele Frequence 0.096845
Functional Annotation downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000527381); intron_variant(ENST00000250379, ENST00000308317, ENST00000396249, ENST00000412033, ENST00000525153, ENST00000531684, ENST00000534684); NMD_transcript_variant(ENST00000412033, ENST00000525153, ENST00000531684); upstream_gene_variant(ENST00000524781, ENST00000524980, ENST00000529365)
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)
GEMIN2 gem (nuclear organelle) associated protein 2 14q21.1 1(0/1/0)

SNPs in LD with rs11157046 (count: 0) View in gBrowse (chr14:39129763..39129763 )

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

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