Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.27 (A)
Location

Chromosome 4:6291188 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs59372792

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

4:g.6291188A>G
ENST00000507765.1:n.646-9A>G
ENST00000503569.5:c.461-9A>G
ENST00000506362.1:c.58-9A>G
ENST00000226760.5:c.461-9A>G

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 3691 sample genotypes, is associated with 3 phenotypes and is mentioned in 82 citations.

Variant displays