SNP Report

Basic Info

Name	rs10467028 dbSNP Ensembl
Location	chr12:106682627 - 106682627(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.355032
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000546882); intron_variant(ENST00000357881, ENST00000392842, ENST00000536688, ENST00000536722, ENST00000539967, ENST00000547531, ENST00000549040, ENST00000549203, ENST00000551505, ENST00000551640); NMD_transcript_variant(ENST00000536722); non_coding_transcript_exon_variant(ENST00000552773); non_coding_transcript_variant(ENST00000536688, ENST00000547531, ENST00000549203, ENST00000551505, ENST00000552773); upstream_gene_variant(ENST00000229387, ENST00000552866, ENST00000552917)
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)
RFX4	regulatory factor X, 4 (influences HLA class II expression)	12q24	2(1/1/0)

SNPs in LD with rs10467028 (count: 0) View in gBrowse (chr12:106682627..106682627 )

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

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