SNP Report

Basic Info

Name	rs6784598 dbSNP Ensembl
Location	chr3:119814409 - 119814409(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.427716
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000474090); intron_variant(ENST00000337940, ENST00000393716, ENST00000466380, ENST00000493757); non_coding_transcript_variant(ENST00000493757)
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)
NR1I2	nuclear receptor subfamily 1, group I, member 2	3q12-q13.3	Mapped by Literature SNP

SNPs in LD with rs6784598 (count: 0) View in gBrowse (chr3:119814409..119814409 )

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

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