SNP Report

Basic Info

Name	rs1573955 dbSNP Ensembl
Location	chr4:118278724 - 118278724(1)
Variant Alleles	G/T
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.352636
Functional Annotation	downstream_gene_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000296498, ENST00000510903); non_coding_transcript_exon_variant(ENST00000602414, ENST00000602520); non_coding_transcript_variant(ENST00000602414, ENST00000602520); upstream_gene_variant(ENST00000384096, ENST00000602483, ENST00000602573, ENST00000602819)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
SNHG8	small nucleolar RNA host gene 8	4q26	Mapped by LD-proxy
PRSS12	protease, serine, 12 (neurotrypsin, motopsin)	4q25-q26	Mapped by LD-proxy

SNPs in LD with rs1573955 (count: 0) View in gBrowse (chr4:118278724..118278724 )

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

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