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rs145088074

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs145088074(A;A)
Make rs145088074(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position38467732
GeneRYR1
is asnp
is mentioned by
dbSNPrs145088074
ebirs145088074
HLIrs145088074
Exacrs145088074
Varsomers145088074
Maprs145088074
PheGenIrs145088074
hapmaprs145088074
1000 genomesrs145088074
hgdprs145088074
ensemblrs145088074
gopubmedrs145088074
geneviewrs145088074
scholarrs145088074
googlers145088074
pharmgkbrs145088074
gwascentralrs145088074
openSNPrs145088074
23andMers145088074
23andMe allrs145088074
SNP Nexus

SNPshotrs145088074
SNPdbers145088074
MSV3drs145088074
GWAS Ctlgrs145088074
Max Magnitude0
ClinVar
Risk rs145088074(A;A)
Alt rs145088074(A;A)
Reference rs145088074(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene RYR1
CLNDBN not specified
Reversed 0
HGVS NC_000019.9:g.38958372G>A
CLNSRC
CLNACC RCV000182605.2,