Original source

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

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

Chromosome 19:46755850 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM033468 ; PhenCode FKRP:c.400C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_051_FKRP_606596_0014, 13924

This variation has 12 HGVS names - click the plus to show

Variation displays