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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57341485

This variant has 2 HGVS names - click the plus to show

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

This variant has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 2510 sample genotypes, is associated with 5 phenotypes and is mentioned in 9 citations.

Variant displays