Original source

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

G/A/T | Ancestral: G | Ambiguity code: D | MAF: 0.08 (T)

Chromosome 1:156134584 (forward strand) | View in location tab


with PhenCode LMNA:c.639+56G>T (G/T)

Most severe consequence
Intron variant
Evidence status

This variant has 3 synonyms - click the plus to show

This variant has 30 HGVS names - click the plus to show

About this variant

This variant overlaps 48 transcripts and has 2507 sample genotypes.

Variant displays