Original source

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

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

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


with COSMIC COSM3750412 (C/T), COSM3750413 (C/T) ; 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

About this variant

This variant overlaps 24 transcripts, has 2323 individual genotypes, is associated with 2 phenotypes and is mentioned in 10 citations.

Variation displays