Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 19:46756349 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM033473 ; PhenCode FKRP:c.899T>C (T/C)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_052_FKRP_606596_0015, 13925

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

Variation displays