Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 15: between 35086857 and 35086858 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB ACTC1_129+23dupC_010411

This variation has 5 HGVS names - click the plus to show

Variation displays