Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

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

Co-located variants

HGMD-PUBLIC CM980494, CM930175

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 16794, 2010_April_001_008_CYP11B1_610613_0003

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