SNP Report

Basic Info

Name	rs2239574 dbSNP Ensembl
Location	chr21:46599898 - 46599898(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.259185
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000291700, ENST00000367071, ENST00000397648)
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)
S100B	S100 calcium binding protein B	21q22.3	2(1/1/0)

SNPs in LD with rs2239574 (count: 0) View in gBrowse (chr21:46599898..46599898 )

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

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