Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 11:112091867 (forward strand) | View in location tab

Most severe consequence

This variation has 13 HGVS names - click the plus to show

Variation displays