SNP Report

Basic Info

Name	rs2942168 dbSNP Ensembl
Location	chrCHR_HSCHR17_2_CTG5:45649105 - 45649105(1)
Variant Alleles	G/A/C/T
Minor Allele	A
Minor Allele Frequence	0.086262
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000444561, ENST00000580220, ENST00000585118, ENST00000585122); intron_variant(ENST00000586362, ENST00000587305, ENST00000591271, ENST00000634540); non_coding_transcript_exon_variant(ENST00000455565); non_coding_transcript_variant(ENST00000455565, ENST00000586362, ENST00000587305, ENST00000591271); upstream_gene_variant(ENST00000578000, ENST00000580655, ENST00000585677, ENST00000592428, ENST00000632092, ENST00000632929, ENST00000633924, ENST00000633957, ENST00000631500, ENST00000632599, ENST00000633119, ENST00000633823, ENST00000631721, ENST00000631500, ENST00000631721, ENST00000632599, ENST00000633119, ENST00000633823, ENST00000632655, ENST00000632912, ENST00000633237, ENST00000634069)
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 rs2942168 (count: 0) View in gBrowse (chrCHR_HSCHR17_2_CTG5:45649105..45649105 )

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

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