Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 9:69065013 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960661

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14155, FRDA_28, 2010_April_001_025_FXN_606829_0004

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

Variation displays