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

Co-located variant

HGMD-PUBLIC CM930178

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 16795, 2010_April_001_009_CYP11B1_610613_0004

HGVS names

This variant has 11 HGVS names - Show

About this variant

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

Variant displays