Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 12:110913117 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB MYL2_381G_A_072611

This variant has 5 HGVS names - click the plus to show

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 2765 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays