Original source

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

Alleles
-/G/GGGGA/GGGGG|MAF: 0.03 (GGGGG)
Location

Chromosome 15: between 34794656 and 34794657 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

LSDB ACTC1_129+23dupC_010411

HGVS names

This variant has 15 HGVS names - Show

About this variant

This variant overlaps 18 transcripts, 1 regulatory feature, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays