Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.28 (C)
Location

Chromosome 4:6293966 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs56732551

This variant has 5 HGVS names - click the plus to show

4:g.6293966C>G
ENST00000507765.1:n.898-1075C>G
ENST00000503569.5:c.713-1075C>G
ENST00000506362.1:c.310-1039C>G
ENST00000226760.5:c.713-1075C>G

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 5 transcripts, has 2783 sample genotypes, is associated with 3 phenotypes and is mentioned in 10 citations.

Variant displays