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 19:46756214 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM033471 ; PhenCode FKRP:c.764G>A (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_050_FKRP_606596_0013, 13923

This variation has 7 HGVS names - click the plus to show

Variation displays