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

rs758925580

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs758925580(C;T)
Make rs758925580(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position38466209
GeneRYR1
is asnp
is mentioned by
dbSNPrs758925580
ebirs758925580
HLIrs758925580
Exacrs758925580
Varsomers758925580
Maprs758925580
PheGenIrs758925580
hapmaprs758925580
1000 genomesrs758925580
hgdprs758925580
ensemblrs758925580
gopubmedrs758925580
geneviewrs758925580
scholarrs758925580
googlers758925580
pharmgkbrs758925580
gwascentralrs758925580
openSNPrs758925580
23andMers758925580
23andMe allrs758925580
SNP Nexus

SNPshotrs758925580
SNPdbers758925580
MSV3drs758925580
GWAS Ctlgrs758925580
Max Magnitude0
ClinVar
Risk rs758925580(T;T)
Alt rs758925580(T;T)
Reference rs758925580(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.38956849C>T
CLNSRC
CLNACC RCV000182603.1,