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)