SNP Report

Basic Info

Name	rs16976931 dbSNP Ensembl
Location	chr18:12006699 - 12006699(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.165935
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000269159, ENST00000383376, ENST00000588752, ENST00000588863, ENST00000588927, ENST00000589238, ENST00000590107, ENST00000590138, ENST00000625802); NMD_transcript_variant(ENST00000383376, ENST00000590107, ENST00000590138); non_coding_transcript_variant(ENST00000588752, ENST00000588863); upstream_gene_variant(ENST00000586230, ENST00000588167)
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 rs16976931 (count: 0) View in gBrowse (chr18:12006699..12006699 )

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

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