SNP Report

Basic Info
Name rs884399 dbSNP Ensembl
Location chr2:45755786 - 45755786(1)
Variant Alleles G/T
Ancestral Allele G
Minor Allele T
Minor Allele Frequence 0.279353
Functional Annotation intron_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000306156, ENST00000421201, ENST00000467135, ENST00000476675, ENST00000480453, ENST00000485176, ENST00000497602); non_coding_transcript_variant(ENST00000467135, ENST00000476675, ENST00000480453, ENST00000485176, ENST00000497602)
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)
PRKCE protein kinase C, epsilon 2p21 1(0/1/0)

SNPs in LD with rs884399 (count: 0) View in gBrowse (chr2:45755786..45755786 )

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

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