Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)
Location

Chromosome 1:156114969 (forward strand) | View in location tab

Co-located

with PhenCode HIFD_LMNA:c.51C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 14 transcripts, has 2540 individual genotypes and is associated with 2 phenotypes.

Variation displays