Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 19:46756403 (forward strand) | View in location tab

Co-located

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

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 13927, 2010_April_001_054_FKRP_606596_0017

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

About this variant

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

Variant displays