SNP Report

Basic Info

Name	rs2839217 dbSNP Ensembl
Location	chr21:46346736 - 46346736(1)
Variant Alleles	G/A/T
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.29992
Functional Annotation	intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; splice_region_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000359568, ENST00000466474, ENST00000480896); non_coding_transcript_exon_variant(ENST00000490468); non_coding_transcript_variant(ENST00000466474, ENST00000480896, ENST00000490468); splice_region_variant(ENST00000359568, ENST00000466474, ENST00000480896); upstream_gene_variant(ENST00000483844)
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)
PCNT	pericentrin	21q22.3	1(0/1/0)

SNPs in LD with rs2839217 (count: 0) View in gBrowse (chr21:46346736..46346736 )

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

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