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 1:156140021 (forward strand) | View in location tab

Co-located

with PhenCode LMNA:c.*915C>T (C/T)

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

LSDB EDMD_46

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 19 transcripts and has 2504 sample genotypes.

Variant displays