Original source

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

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

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

Most severe consequence
Intron variant
Evidence status

Clinical significance


LSDB MYH7_1408-42delC_010411

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 2 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays