SNP Report

Basic Info

Name	rs583965 dbSNP Ensembl
Location	chr18:12026504 - 12026504(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.464457
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000587619); intron_variant(ENST00000269159, ENST00000586230, ENST00000588167, ENST00000588752, ENST00000588927, ENST00000589238, ENST00000590107, ENST00000590138); NMD_transcript_variant(ENST00000586230, ENST00000590107, ENST00000590138); non_coding_transcript_variant(ENST00000588167, ENST00000588752); upstream_gene_variant(ENST00000589374)
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)
IMPA2	inositol(myo)-1(or 4)-monophosphatase 2	18p11.2	4(2/2/0)

SNPs in LD with rs583965 (count: 0) View in gBrowse (chr18:12026504..12026504 )

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

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