Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H | MAF: < 0.01 (T)
Location

Chromosome 19:46756604 (forward strand) | View in location tab

Co-located

with COSMIC COSM3536208 (C/T) ; HGMD-PUBLIC CM013810 ; PhenCode FKRP:c.1154C>A (C/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_040_FKRP_606596_0002, 13912

This variation has 14 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

Variation displays