Original source

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

Alleles
C/T | Ambiguity code: Y
Location

Chromosome 8:142875712 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930178

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16795, 2010_April_001_009_CYP11B1_610613_0004

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

Variation displays