SNP Report

Basic Info
Name rs6022787 dbSNP Ensembl
Location chr20:38068801 - 38068801(1)
Variant Alleles G/C
Ancestral Allele C
Minor Allele G
Minor Allele Frequence 0.365216
Functional Annotation intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000373433, ENST00000449186, ENST00000462548, ENST00000614670, ENST00000618318, ENST00000622494); NMD_transcript_variant(ENST00000462548); non_coding_transcript_variant(ENST00000618318)
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)
RPRD1B regulation of nuclear pre-mRNA domain containing 1B 20q11.23 Mapped by Literature SNP

SNPs in LD with rs6022787 (count: 0) View in gBrowse (chr20:38068801..38068801 )

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

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