SNP Report

Basic Info

Name	rs1042356 dbSNP Ensembl
Location	chr17:6999424 - 6999424(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.398163
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; synonymous_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000399540, ENST00000573939); intron_variant(ENST00000399541, ENST00000570562, ENST00000572385, ENST00000572547, ENST00000575889); non_coding_transcript_exon_variant(ENST00000571010, ENST00000574377, ENST00000575727); non_coding_transcript_variant(ENST00000399541, ENST00000570562, ENST00000571010, ENST00000572385, ENST00000572547, ENST00000574377, ENST00000575727, ENST00000575889); synonymous_variant(ENST00000251535, ENST00000480801); upstream_gene_variant(ENST00000573222)
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)
ALOX12	arachidonate 12-lipoxygenase	17p13.1	2(1/1/0)

SNPs in LD with rs1042356 (count: 0) View in gBrowse (chr17:6999424..6999424 )

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

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