Original source

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

Alleles
G/T | Ambiguity code: K
Location

Chromosome 8:142875730 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM062570

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16808, 2010_April_001_015_CYP11B1_610613_0017

This variation has 11 HGVS names - click the plus to show

Variation displays