SNP Report

Basic Info

Name	rs8034542 dbSNP Ensembl
Location	chr15:78936029 - 78936029(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.160343
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000528436, ENST00000534268); intron_variant(ENST00000220166, ENST00000525807, ENST00000528191, ENST00000528741, ENST00000529263, ENST00000529861, ENST00000530010, ENST00000530929, ENST00000533777, ENST00000534038, ENST00000534533, ENST00000615999); NMD_transcript_variant(ENST00000525807, ENST00000529861, ENST00000533777); non_coding_transcript_variant(ENST00000528191, ENST00000529263, ENST00000530010, ENST00000530929, ENST00000534038, ENST00000534533); upstream_gene_variant(ENST00000527138, ENST00000529612, ENST00000534237)
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 rs8034542 (count: 0) View in gBrowse (chr15:78936029..78936029 )

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

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