Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057524858

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524858(A;A)
Make rs1057524858(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position38502728
GeneRYR1
is asnp
is mentioned by
dbSNPrs1057524858
dbSNP (old)rs1057524858
ClinGenrs1057524858
ebirs1057524858
HLIrs1057524858
Exacrs1057524858
Gnomadrs1057524858
Varsomers1057524858
LitVarrs1057524858
Maprs1057524858
PheGenIrs1057524858
Biobankrs1057524858
1000 genomesrs1057524858
hgdprs1057524858
ensemblrs1057524858
gopubmedrs1057524858
geneviewrs1057524858
scholarrs1057524858
googlers1057524858
pharmgkbrs1057524858
gwascentralrs1057524858
openSNPrs1057524858
23andMers1057524858
23andMe allrs1057524858
SNPshotrs1057524858
SNPdbers1057524858
MSV3drs1057524858
GWAS Ctlgrs1057524858
Max Magnitude0
ClinVar
Risk rs1057524858(A;A)
Alt rs1057524858(A;A)
Reference Rs1057524858(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.38993368G>A
CLNSRC
CLNACC RCV000442837.1,