SNP Report

Basic Info

Name	rs11111882 dbSNP Ensembl
Location	chr12:104061562 - 104061562(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.151558
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000548660); upstream_gene_variant(ENST00000229330, ENST00000544223, ENST00000550444)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
HCFC2	host cell factor C2	12q23.3	Mapped by LD-proxy
GLT8D2	glycosyltransferase 8 domain containing 2	12q23.3	Mapped by LD-proxy

SNPs in LD with rs11111882 (count: 0) View in gBrowse (chr12:104061562..104061562 )

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

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