Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57341485

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

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

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

Variation displays