SNP Report

Basic Info

Name	rs1044431 dbSNP Ensembl
Location	chr11:13388296 - 13388296(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.147364
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; NMD_transcript_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000278174, ENST00000527102); downstream_gene_variant(ENST00000389707, ENST00000401424, ENST00000403290, ENST00000403482, ENST00000403510, ENST00000472842, ENST00000524392, ENST00000528120, ENST00000530907); NMD_transcript_variant(ENST00000527102)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
ARNTL	aryl hydrocarbon receptor nuclear translocator-like	11p15	7(5/2/0)
BTBD10	BTB (POZ) domain containing 10	11p15.2	Mapped by Literature SNP

SNPs in LD with rs1044431 (count: 0) View in gBrowse (chr11:13388296..13388296 )

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

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