Original source

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

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

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

Co-located variant

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

Most severe consequence
 
Missense variant
Evidence status

Synonyms

LSDB EDMD_6

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and 1 regulatory feature.

Variant displays