Original source

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

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

Chromosome 1:156134888 (forward strand)|View in location tab

Co-located variant

PhenCode HIFD_LMNA:c.723G>A (G/A)

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB EDMD_18, LMNA:c.723G>A

HGVS names

This variant has 29 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and is associated with 1 phenotype.

Variant displays