Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 1:156134856 (forward strand) | View in location tab

Co-located

with PhenCode LMNA:c.691A>C (A/C)

Most severe consequence
 
Missense variant
Synonyms

LSDB EDMD_17

This variant has 29 HGVS names - click the plus to show

About this variant

This variant overlaps 24 transcripts and has 262 sample genotypes.

Variant displays