Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/G/T | Ancestral: C | Ambiguity code: B | MAF: 0.03 (T)

Chromosome 19:38500960 (forward strand) | View in location tab


with PhenCode RYR1:c.7584C>T (C/T)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance

HGVS names

This variant has 24 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2542 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays