Original source

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

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

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

Co-located variants

COSMIC COSM5009874 ; PhenCode RYR1:c.7584C>T (C/T)

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms
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 2 phenotypes and is mentioned in 1 citation.

Variant displays