SNP Report

Basic Info

Name	rs4979328 dbSNP Ensembl
Location	chr9:114026134 - 114026134(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.245208
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000288466, ENST00000374124, ENST00000374126, ENST00000452710, ENST00000481558, ENST00000615615); non_coding_transcript_variant(ENST00000481558); upstream_gene_variant(ENST00000470105)
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)
ZNF618	zinc finger protein 618	9q33.1	Mapped by Literature SNP

SNPs in LD with rs4979328 (count: 0) View in gBrowse (chr9:114026134..114026134 )

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

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