Original source

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

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

Chromosome 1:156114923 (forward strand) | View in location tab

Co-located

with PhenCode LMNA:c.5A>G (A/G)

Most severe consequence
Evidence status

Synonyms

LSDB EDMD_6

This variation has 22 HGVS names - click the plus to show

Variation displays