Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.08 (T)

Chromosome 1:156134601 (forward strand) | View in location tab


with PhenCode LMNA:c.639+73C>T (C/T)

Most severe consequence
Intron variant
Evidence status

This variant has 2 synonyms - click the plus to show

This variant has 15 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 24 transcripts and has 2506 sample genotypes.

Variant displays