Original source

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

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

Chromosome 13:20223467 (forward strand) | View in location tab

Co-located

with COSMIC COSM945876 (G/A) ; HGMD-PUBLIC CM993506

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_050_GJB6_604418_0001, 12666

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

Genotyping chips

This variation has assays on: HumanCoreExome-12

Variation displays