SNP Report

Basic Info

Name	rs909859 dbSNP Ensembl
Location	chr20:38109720 - 38109720(1)
Variant Alleles	G/C
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.361621
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000614670, ENST00000618318); non_coding_transcript_variant(ENST00000618318); upstream_gene_variant(ENST00000615357)
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 rs909859 (count: 0) View in gBrowse (chr20:38109720..38109720 )

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

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