Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)

Chromosome 1:156114969 (forward strand) | View in location tab


with PhenCode HIFD_LMNA:c.51C>T (C/T)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 13 transcripts, 1 regulatory feature, has 2540 sample genotypes and is associated with 2 phenotypes.

Variant displays