SNP Report

Basic Info

Name	rs906190 dbSNP Ensembl
Location	chr19:50994163 - 50994163(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.314696
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000291726, ENST00000320838, ENST00000347619, ENST00000391806, ENST00000593490, ENST00000594669, ENST00000594914, ENST00000598195, ENST00000599166, ENST00000600767); intron_variant(ENST00000594512); non_coding_transcript_variant(ENST00000594512)
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)
KLK8	kallikrein-related peptidase 8	19q13	1(1/0/0)

SNPs in LD with rs906190 (count: 0) View in gBrowse (chr19:50994163..50994163 )

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

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