Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variants

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

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_051_FKRP_606596_0014, 13924

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and is associated with 2 phenotypes.

Variant displays