Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 19:47259660 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM040993 ; PhenCode FKRP:c.953G>A (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13927, 2010_April_001_054_FKRP_606596_0017

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

Variation displays