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 | MAF: 0.06 (T)

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


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

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

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

About this variant

This variant overlaps 48 transcripts and has 1095 individual genotypes.

Variation displays