Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.08 (T)
Location

Chromosome 1:156134601 (forward strand)|View in location tab

Co-located variant

PhenCode LMNA:c.639+73C>T (C/T)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 15 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 24 transcripts and has 2506 sample genotypes.

Variant displays