SNP Report

Basic Info
Name rs910664 dbSNP Ensembl
Location chr20:38053899 - 38053899(1)
Variant Alleles C/T
Ancestral Allele T
Minor Allele C
Minor Allele Frequence 0.365016
Functional Annotation intron_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000373433, ENST00000449186, ENST00000462548, ENST00000495457); NMD_transcript_variant(ENST00000462548, ENST00000495457)
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 rs910664 (count: 0) View in gBrowse (chr20:38053899..38053899 )

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

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