SNP Report

Basic Info

Name	rs916782 dbSNP Ensembl
Location	chr22:30079103 - 30079103(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.0926518
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000429350, ENST00000432568, ENST00000453743); non_coding_transcript_variant(ENST00000429350, ENST00000432568, ENST00000453743); upstream_gene_variant(ENST00000336726, ENST00000403975, ENST00000450612)
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)
HORMAD2	HORMA domain containing 2	22q12.2	Mapped by LD-proxy

SNPs in LD with rs916782 (count: 0) View in gBrowse (chr22:30079103..30079103 )

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

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