SNP Report

Basic Info

Name	rs2289695 dbSNP Ensembl
Location	chr15:78925289 - 78925289(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.132188
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000527138, ENST00000528741, ENST00000529263, ENST00000529612, ENST00000529861); intron_variant(ENST00000220166, ENST00000525807, ENST00000527715, ENST00000533777, ENST00000534237, ENST00000534533, ENST00000615999); NMD_transcript_variant(ENST00000525807, ENST00000533777); non_coding_transcript_variant(ENST00000527715, ENST00000534237, ENST00000534533)
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)
CTSH	cathepsin H	15q25.1	1(0/0/1)

SNPs in LD with rs2289695 (count: 0) View in gBrowse (chr15:78925289..78925289 )

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

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