Original source

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

Alleles
G/A | Ambiguity code: R
Location

Chromosome 8:142879690 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970405

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB CYP11B1_124C_T_020111, 16800, 2010_April_001_013_CYP11B1_610613_0009

This variation has 9 HGVS names - click the plus to show

Variation displays