Original source

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

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

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


with HGMD-PUBLIC CM970534

Most severe consequence
Evidence status

Clinical significance


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, HumanCoreExome-12

About this variant

This variant overlaps 5 transcripts, is associated with 2 phenotypes and is mentioned in 2 citations.

Variation displays