Original source

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

Alleles
G/C/T | Ancestral: G | Ambiguity code: B
Location

Chromosome 4:54967798 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 12 HGVS names - click the plus to show

Variation displays