Original source

Variants (including SNPs and indels) imported from dbSNP [remapped from build CAT] (release 127) | [View in dbSNP]

Alleles
G/A | Ambiguity code: R
Location

Chromosome A1:10132487 (forward strand) | View in location tab

Most severe consequence

This variation has 5 HGVS names - click the plus to show

Variation displays