SNP Report

Basic Info

Name	rs2087439 dbSNP Ensembl
Location	chr4:117651630 - 117651630(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.139577
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000422145, ENST00000600624, ENST00000615833, ENST00000626258); non_coding_transcript_variant(ENST00000422145, ENST00000600624, ENST00000615833, ENST00000626258); upstream_gene_variant(ENST00000630321)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 0)

SNPs in LD with rs2087439 (count: 0) View in gBrowse (chr4:117651630..117651630 )

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

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