Original source

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

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

Chromosome 10:102832610 (forward strand) | View in location tab

Co-located

with COSMIC COSM1345509 (C/T) ; HGMD-PUBLIC CM960476

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_010_CYP17A1_609300_0012, 16224

This variation has 3 HGVS names - click the plus to show

Variation displays