SNP Report

Basic Info

Name	rs2837596 dbSNP Ensembl
Location	chr21:40383482 - 40383482(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.145567
Functional Annotation	intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000400454, ENST00000422749, ENST00000427451, ENST00000444046); non_coding_transcript_exon_variant(ENST00000455354); non_coding_transcript_variant(ENST00000422749, ENST00000427451, ENST00000444046, ENST00000455354)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

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)
DSCAM-AS1	DSCAM antisense RNA 1	21q22.2	Mapped by LD-proxy

SNPs in LD with rs2837596 (count: 0) View in gBrowse (chr21:40383482..40383482 )

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

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