Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variant

HGMD-PUBLIC CM930173

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 16797, 2010_April_001_010_CYP11B1_610613_0006

HGVS names

This variant has 9 HGVS names - Show

About this variant

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

Variant displays