Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/- | Ancestral: G | MAF: 0.01 (-)
Location

Chromosome 14:23428712 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB MYH7_1408-42delC_010411

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 2504 individual genotypes and is associated with 1 phenotype.

Variation displays