Original source

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

Alleles
T/C/G | Ambiguity code: B
Location

Chromosome 8:142877221 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970406

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16798, 2010_April_001_011_CYP11B1_610613_0007

This variation has 18 HGVS names - click the plus to show

Variation displays