Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A | Ambiguity code: R
Location

Chromosome 8:142875877 (forward strand) | View in location tab

Co-located

with COSMIC COSM205557 (G/A) ; HGMD-PUBLIC CM970407

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_012_CYP11B1_610613_0008, 16799

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

Variation displays