SNP Report

Basic Info

Name	rs17090376 dbSNP Ensembl
Location	chr18:56837597 - 56837597(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.0183706
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000254442, ENST00000357574, ENST00000589935, ENST00000615645)
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)
WDR7	WD repeat domain 7	18q21.31	1(0/1/0)

SNPs in LD with rs17090376 (count: 0) View in gBrowse (chr18:56837597..56837597 )

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

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