Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.04 (A)
Location

Chromosome 14:23402700 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB MYH6_999C_T_090710

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts, has 2506 individual genotypes and is associated with 1 phenotype.

Variation displays