SNP Report

Basic Info

Name	rs418891 dbSNP Ensembl
Location	chrCHR_HSCHR17_2_CTG5:45627805 - 45627805(1)
Variant Alleles	G/T
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.0864617
Functional Annotation	upstream_gene_variant.
Consequence to Transcript	upstream_gene_variant(ENST00000455565, ENST00000582491, ENST00000583740, ENST00000585118, ENST00000585122, ENST00000591271, ENST00000634540, ENST00000631721, ENST00000632092, ENST00000632544, ENST00000632929, ENST00000633571, ENST00000633823)
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)
CRHR1-IT1	CRHR1 intronic transcript 1	17q21.31	Mapped by LD-proxy

SNPs in LD with rs418891 (count: 0) View in gBrowse (chrCHR_HSCHR17_2_CTG5:45627805..45627805 )

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

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