SNP Report

Basic Info

Name	rs381493 dbSNP Ensembl
Location	chrCHR_HSCHR6_MHC_COX_CTG1:28590474 - 28590474(1)
Variant Alleles	A/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.0485224
Functional Annotation	intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000530247); non_coding_transcript_exon_variant(ENST00000499525); non_coding_transcript_variant(ENST00000499525, ENST00000530247); upstream_gene_variant(ENST00000452236, ENST00000524745, ENST00000526291, ENST00000619431, ENST00000619431, ENST00000508341)
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)
SCAND3	zinc finger, BED-type containing 9	6p21.33	Mapped by LD-proxy

SNPs in LD with rs381493 (count: 0) View in gBrowse (chrCHR_HSCHR6_MHC_COX_CTG1:28590474..28590474 )

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

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