SNP Report

Basic Info

Name	rs436667 dbSNP Ensembl
Location	chrCHR_HSCHR17_2_CTG5:45643670 - 45643670(1)
Variant Alleles	C/T
Minor Allele	T
Minor Allele Frequence	0.0860623
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000582491, ENST00000583740); intron_variant(ENST00000455565, ENST00000580220, ENST00000585118, ENST00000585122, ENST00000587305, ENST00000591271, ENST00000634540); non_coding_transcript_variant(ENST00000455565, ENST00000580220, ENST00000585118, ENST00000585122, ENST00000587305, ENST00000591271); upstream_gene_variant(ENST00000444561, ENST00000632544, ENST00000633571, ENST00000631500, ENST00000631721, ENST00000632092, ENST00000632599, ENST00000632929, ENST00000633823, ENST00000633924, ENST00000631500, ENST00000631721, ENST00000632092, ENST00000632599, ENST00000632929, ENST00000633823, ENST00000633924, ENST00000633957)
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 rs436667 (count: 0) View in gBrowse (chrCHR_HSCHR17_2_CTG5:45643670..45643670 )

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

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