Original source

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

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

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

Co-located variant

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

Most severe consequence
Intron variant
Evidence status


This variant has 3 synonyms - Show

HGVS names

This variant has 30 HGVS names - Show

About this variant

This variant overlaps 48 transcripts and has 2507 sample genotypes.

Variant displays