Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

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

Co-located

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

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and is associated with 4 phenotypes.

Variant displays