Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.19 (T)
Location

Chromosome 19:38434174 (forward strand) | View in location tab

Co-located

with PhenCode RYR1:c.45+300T>C (T/C)

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 4 HGVS names - click the plus to show

This variant has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 3695 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays