SNP Report

Basic Info

Name	rs129982 dbSNP Ensembl
Location	chr16:3751648 - 3751648(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.103035
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000262367, ENST00000382070, ENST00000570939, ENST00000573517); upstream_gene_variant(ENST00000638158)
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)
CREBBP	CREB binding protein	16p13.3	1(0/1/0)

SNPs in LD with rs129982 (count: 0) View in gBrowse (chr16:3751648..3751648 )

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

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