SNP Report

Basic Info

Name	rs2001893 dbSNP Ensembl
Location	chr10:35011695 - 35011695(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.364417
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000374746, ENST00000374748, ENST00000374749, ENST00000374751, ENST00000374754, ENST00000421317, ENST00000537177, ENST00000626172); NMD_transcript_variant(ENST00000374754)
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)
CUL2	cullin 2	10p11.2	Mapped by LD-proxy

SNPs in LD with rs2001893 (count: 0) View in gBrowse (chr10:35011695..35011695 )

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

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