SNP Report

Basic Info

Name	rs2839262 dbSNP Ensembl
Location	chr21:46442711 - 46442711(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.185304
Functional Annotation	intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000359568, ENST00000418394, ENST00000480896); non_coding_transcript_exon_variant(ENST00000465356); non_coding_transcript_variant(ENST00000465356, ENST00000480896)
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 rs2839262 (count: 0) View in gBrowse (chr21:46442711..46442711 )

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

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