Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/G/T | Ancestral: G | Ambiguity code: D | MAF: 0.41 (A)
Location

Chromosome 11:18424487 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 34 HGVS names - click the plus to show

Variation displays