SNP Report

Basic Info

Name	rs10849930 dbSNP Ensembl
Location	chr12:111301432 - 111301432(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.410343
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000261726); upstream_gene_variant(ENST00000617342)
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)
CUX2	cut-like homeobox 2	12q24.12	3(1/2/0)

SNPs in LD with rs10849930 (count: 0) View in gBrowse (chr12:111301432..111301432 )

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

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