SNP Report

Basic Info

Name	rs2272789 dbSNP Ensembl
Location	chr22:35283958 - 35283958(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.446086
Functional Annotation	intron_variant; NMD_transcript_variant; splice_region_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000216106, ENST00000418170); NMD_transcript_variant(ENST00000418170); splice_region_variant(ENST00000216106, ENST00000418170); upstream_gene_variant(ENST00000498212)
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)
HMGXB4	HMG box domain containing 4	22q13	1(1/0/0)

SNPs in LD with rs2272789 (count: 0) View in gBrowse (chr22:35283958..35283958 )

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

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