SNP Report

Basic Info

Name	rs2942164 dbSNP Ensembl
Location	chrCHR_HSCHR17_2_CTG5:45655542 - 45655542(1)
Variant Alleles	G/C
Minor Allele	C
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(ENST00000578000, ENST00000580655); intron_variant(ENST00000585677, ENST00000586362, ENST00000587305, ENST00000591271, ENST00000592428, ENST00000634540); non_coding_transcript_variant(ENST00000585677, ENST00000586362, ENST00000587305, ENST00000591271, ENST00000592428); upstream_gene_variant(ENST00000589868, ENST00000633237, ENST00000634069, ENST00000631500, ENST00000632599, ENST00000632655, ENST00000632912, ENST00000633119, ENST00000633823, ENST00000631500, ENST00000632599, ENST00000632655, ENST00000632912, ENST00000633119, ENST00000633823, ENST00000633111)
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 rs2942164 (count: 0) View in gBrowse (chrCHR_HSCHR17_2_CTG5:45655542..45655542 )

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

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