SNP Report

Basic Info

Name	rs1562436 dbSNP Ensembl
Location	chr11:13440509 - 13440509(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.42472
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000527858); intron_variant(ENST00000278174, ENST00000525108, ENST00000525864, ENST00000526841, ENST00000527102, ENST00000528120, ENST00000529708); NMD_transcript_variant(ENST00000525108, ENST00000527102); non_coding_transcript_variant(ENST00000525864); upstream_gene_variant(ENST00000525661, ENST00000530907, ENST00000532261)
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)
BTBD10	BTB (POZ) domain containing 10	11p15.2	Mapped by Literature SNP

SNPs in LD with rs1562436 (count: 0) View in gBrowse (chr11:13440509..13440509 )

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

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