SNP Report

Basic Info

Name	rs12626191 dbSNP Ensembl
Location	chr21:46656451 - 46656451(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.22504
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000334494, ENST00000455177); intron_variant(ENST00000291705, ENST00000355680, ENST00000397637, ENST00000397638, ENST00000440086, ENST00000451211, ENST00000458387, ENST00000481861, ENST00000482508, ENST00000621201); non_coding_transcript_variant(ENST00000481861, ENST00000482508); upstream_gene_variant(ENST00000419906, ENST00000486520)
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)
DSTNP1	destrin (actin depolymerizing factor) pseudogene 1	21q22.3	Mapped by LD-proxy
PRMT2	protein arginine methyltransferase 2	21q22.3	Mapped by LD-proxy

SNPs in LD with rs12626191 (count: 0) View in gBrowse (chr21:46656451..46656451 )

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

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