SNP Report

Basic Info

Name	rs1044314 dbSNP Ensembl
Location	chr11:125431909 - 125431909(1)
Variant Alleles	G/T
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.322484
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000298282); downstream_gene_variant(ENST00000530517, ENST00000531116, ENST00000532623); non_coding_transcript_exon_variant(ENST00000526955); non_coding_transcript_variant(ENST00000526955)
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)
PKNOX2	PBX/knotted 1 homeobox 2	11q24.2	Mapped by LD-proxy

SNPs in LD with rs1044314 (count: 0) View in gBrowse (chr11:125431909..125431909 )

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

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