Original source

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

Alleles
G/A | Ancestral: C | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 8:128425906 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 4 HGVS names - click the plus to show

Variation displays