Original source

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

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

Chromosome 12:110913097 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM086879

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB MYL2_00014_DUPLOCSNPID_1

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

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

Variation displays