SNP Report

Basic Info

Name	rs2043885 dbSNP Ensembl
Location	chr2:124098762 - 124098762(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.365615
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000423939, ENST00000431078); non_coding_transcript_variant(ENST00000423939)
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)
CNTNAP5	contactin associated protein-like 5	2q14.1	2(0/2/0)

SNPs in LD with rs2043885 (count: 0) View in gBrowse (chr2:124098762..124098762 )

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

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