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)