Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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 variant

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

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

LSDB EDMD_46

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 19 transcripts and has 2504 sample genotypes.

Variant displays