Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 1:156134888 (forward strand) | View in location tab

Co-located

with PhenCode HIFD_LMNA:c.723G>A (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB LMNA:c.723G>A, EDMD_18

This variation has 17 HGVS names - click the plus to show

Variation displays