SNP Report

Basic Info

Name	rs6058339 dbSNP Ensembl
Location	chr20:35872557 - 35872557(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.0265575
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000485604, ENST00000486408); intron_variant(ENST00000339089, ENST00000374000, ENST00000374012, ENST00000481202, ENST00000495338); non_coding_transcript_variant(ENST00000481202, ENST00000495338)
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)
PHF20	PHD finger protein 20	20q11.22-q11.23	1(0/1/0)

SNPs in LD with rs6058339 (count: 0) View in gBrowse (chr20:35872557..35872557 )

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

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