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 8:142876242 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980494, CM930175

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16794, 2010_April_001_008_CYP11B1_610613_0003

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

Variation displays