Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.01 (A)

Chromosome 1:156134501 (forward strand) | View in location tab


with PhenCode HIFD_LMNA:c.612G>A (G/A)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 28 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 24 transcripts, has 3274 sample genotypes and is associated with 1 phenotype.

Variant displays