Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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

Variation displays