Original source

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

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

Chromosome 1:156114923 (forward strand) | View in location tab

Co-located

with PhenCode LMNA:c.5A>G (A/G)

Most severe consequence
 
Missense variant
Synonyms

LSDB EDMD_6

This variant has 22 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and 1 regulatory feature.

Variant displays