Original source

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

Alleles
C/A/T|Ancestral: C|Ambiguity code: H
Location

Chromosome 19:2434029 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM062823 ; PhenCode HIFD_LMNB2:c.1219G>A (C/T)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and is associated with 4 phenotypes.

Variant displays