SNP Report

Basic Info

Name	rs17001167 dbSNP Ensembl
Location	chr22:39485135 - 39485135(1)
Variant Alleles	T/G
Ancestral Allele	T
Minor Allele	G
Minor Allele Frequence	0.103035
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000341184, ENST00000418314, ENST00000429402)
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)
MGAT3	mannosyl (beta-1,4-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase	22q13.1	Mapped by LD-proxy

SNPs in LD with rs17001167 (count: 0) View in gBrowse (chr22:39485135..39485135 )

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

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