Original source

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

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

Chromosome 1:237798109 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


LSDB RYR2_14029C_T_011211

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts, has 2505 sample genotypes and is associated with 2 phenotypes.

Variant displays