Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

Chromosome 6:33572432 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57341485

HGVS names

This variant has 2 HGVS names - Hide

6:g.33572432A>G
ENST00000612409.1:n.248+1621A>G

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 4 transcripts, has 4204 sample genotypes, is associated with 5 phenotypes and is mentioned in 9 citations.

Variant displays