Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.21 (T)
Location

Chromosome 1:156137743 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM003892 ; PhenCode HIFD_LMNA:c.1698C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

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

This variation has assays on 7 chips - click the plus to show

Variation displays