SNP Report

Basic Info

Name	rs11637890 dbSNP Ensembl
Location	chr15:78643077 - 78643077(1)
Variant Alleles	C/G
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.20627
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000559849, ENST00000560511); NMD_transcript_variant(ENST00000559849); non_coding_transcript_variant(ENST00000560511); upstream_gene_variant(ENST00000261751, ENST00000412074)
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)
CHRNB4	cholinergic receptor, nicotinic, beta 4 (neuronal)	15q24	2(1/1/0)

SNPs in LD with rs11637890 (count: 0) View in gBrowse (chr15:78643077..78643077 )

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

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