SNP Report

Basic Info

Name	rs2839250 dbSNP Ensembl
Location	chr21:46421640 - 46421640(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.331669
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000359568, ENST00000480896); non_coding_transcript_variant(ENST00000480896); upstream_gene_variant(ENST00000450007)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
PCNT	pericentrin	21q22.3	1(0/1/0)
RPL18AP2	ribosomal protein L18a pseudogene 2	21q22.3	Mapped by Literature SNP

SNPs in LD with rs2839250 (count: 0) View in gBrowse (chr21:46421640..46421640 )

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

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