Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 9:69064942 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970534

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14156, FRDA_25, 2010_April_001_026_FXN_606829_0005

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays