SNP Report

Basic Info

Name	rs10776586 dbSNP Ensembl
Location	chr10:49650300 - 49650300(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.351637
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000337653, ENST00000339797, ENST00000351556, ENST00000395559, ENST00000395562, ENST00000466590); NMD_transcript_variant(ENST00000466590)
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)
CHAT	choline O-acetyltransferase	10q11.2	1(0/1/0)

SNPs in LD with rs10776586 (count: 0) View in gBrowse (chr10:49650300..49650300 )

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

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