SNP Report

Basic Info

Name	rs1551067 dbSNP Ensembl
Location	chrCHR_HG2191_PATCH:75029427 - 75029427(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.459065
Functional Annotation	downstream_gene_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000490365); intron_variant(ENST00000287239, ENST00000372711, ENST00000372714, ENST00000372724, ENST00000372725); upstream_gene_variant(ENST00000413431, ENST00000436608, ENST00000626984, ENST00000628038, ENST00000628523, ENST00000629233, ENST00000629879, ENST00000630001, ENST00000628094, ENST00000629818)
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)
KAT6B	K(lysine) acetyltransferase 6B	10q22.2	1(1/0/0)

SNPs in LD with rs1551067 (count: 0) View in gBrowse (chrCHR_HG2191_PATCH:75029427..75029427 )

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

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