Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 8:142879080 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930173

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16797, 2010_April_001_010_CYP11B1_610613_0006

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

About this variant

This variant overlaps 6 transcripts and is associated with 2 phenotypes.

Variation displays