SNP Report

Basic Info

Name	rs1029871 dbSNP Ensembl
Location	chr3:52763618 - 52763618(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.30631
Functional Annotation	downstream_gene_variant; missense_variant. Polyphen Annotation: possibly damaging(ENST00000233027, ENST00000383721); probably damaging(ENST00000461689, ENST00000535191) SIFT Annotation: deleterious(ENST00000461689, ENST00000535191); tolerated(ENST00000233027, ENST00000383721)
Consequence to Transcript	downstream_gene_variant(ENST00000496822); missense_variant(ENST00000233027, ENST00000383721, ENST00000461689, ENST00000535191)
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)
NEK4	NIMA-related kinase 4	3p21.1	1(1/0/0)

SNPs in LD with rs1029871 (count: 0) View in gBrowse (chr3:52763618..52763618 )

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

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