SNP Report

Basic Info
Name rs2980623 dbSNP Ensembl
Location chr8:109296099 - 109296099(1)
Variant Alleles C/T
Ancestral Allele T
Minor Allele C
Minor Allele Frequence 0.326078
Functional Annotation intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000239690, ENST00000427660, ENST00000519607, ENST00000521439); NMD_transcript_variant(ENST00000519607, ENST00000521439); upstream_gene_variant(ENST00000504175)
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)
NUDCD1 NudC domain containing 1 8q23 1(0/1/0)

SNPs in LD with rs2980623 (count: 0) View in gBrowse (chr8:109296099..109296099 )

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

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