Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 14:23418398 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM050708

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB MYH7_3981C_A_061711

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

About this variant

This variant overlaps 4 transcripts, is associated with 1 phenotype and is mentioned in 2 citations.

Variation displays