Original source

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

A/C/G | Ancestral: C | Ambiguity code: V | MAF: < 0.01 (C)

Chromosome 14:23387882 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


LSDB MYH6_4401T_G_022311

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 8 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays