SNP Report

Basic Info

Name	rs11911000 dbSNP Ensembl
Location	chr21:40051885 - 40051885(1)
Variant Alleles	G/T
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.110024
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000400454, ENST00000404019, ENST00000617870)
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)
DSCAM	Down syndrome cell adhesion molecule	21q22.2-q22.3	3(1/2/0)

SNPs in LD with rs11911000 (count: 0) View in gBrowse (chr21:40051885..40051885 )

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

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