Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

G/A/T | Ancestral: G | Ambiguity code: D

Chromosome 1:156138660 (forward strand) | View in location tab


with COSMIC COSM4023189 (G/A) ; HGMD-PUBLIC CM020736 ; PhenCode HIFD_LMNA:c.1871G>A (G/A), LMNA:c.1871G>T (G/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 38 HGVS names - click the plus to show

About this variant

This variant overlaps 48 transcripts, has 2 individual genotypes and is associated with 1 phenotype.

Variation displays