Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 1:156134856 (forward strand) | View in location tab

Co-located

with PhenCode LMNA:c.691A>C (A/C)

Most severe consequence
Evidence status

Synonyms

LSDB EDMD_17

This variation has 29 HGVS names - click the plus to show

Variation displays