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

Co-located

with HGMD-PUBLIC CM930178

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16795, 2010_April_001_009_CYP11B1_610613_0004

This variation has 11 HGVS names - click the plus to show

About this variant

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

Variation displays