Original source

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

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

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

Co-located variant

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

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 13 transcripts, 1 regulatory feature, has 2540 sample genotypes and is associated with 3 phenotypes.

Variant displays