SNP Report

Basic Info

Name	rs12906951 dbSNP Ensembl
Location	chr15:78533220 - 78533220(1)
Variant Alleles	C/A/T
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.236222
Functional Annotation	downstream_gene_variant; intron_variant; missense_variant; synonymous_variant; upstream_gene_variant. Polyphen Annotation: probably damaging(ENST00000388988, ENST00000569878) SIFT Annotation: deleterious(ENST00000388988, ENST00000569878)
Consequence to Transcript	downstream_gene_variant(ENST00000566289, ENST00000566332); intron_variant(ENST00000408962, ENST00000563233); missense_variant(ENST00000388988, ENST00000569878); synonymous_variant(ENST00000388988, ENST00000569878); upstream_gene_variant(ENST00000623556)
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)
HYKK	hydroxylysine kinase	15q25.1	Mapped by LD-proxy

SNPs in LD with rs12906951 (count: 0) View in gBrowse (chr15:78533220..78533220 )

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

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