SNP Report

Basic Info

Name	rs3761219 dbSNP Ensembl
Location	chr20:3795721 - 3795721(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.295327
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000344256, ENST00000379598); upstream_gene_variant(ENST00000245960, ENST00000340833, ENST00000439880, ENST00000467519)
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)
CDC25B	cell division cycle 25B	20p13	1(0/1/0)

SNPs in LD with rs3761219 (count: 0) View in gBrowse (chr20:3795721..3795721 )

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

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