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

rs760010175

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs760010175(A;A)
Make rs760010175(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position38585949
GeneRYR1
is asnp
is mentioned by
dbSNPrs760010175
ebirs760010175
HLIrs760010175
Exacrs760010175
Varsomers760010175
Maprs760010175
PheGenIrs760010175
hapmaprs760010175
1000 genomesrs760010175
hgdprs760010175
ensemblrs760010175
gopubmedrs760010175
geneviewrs760010175
scholarrs760010175
googlers760010175
pharmgkbrs760010175
gwascentralrs760010175
openSNPrs760010175
23andMers760010175
23andMe allrs760010175
SNP Nexus

SNPshotrs760010175
SNPdbers760010175
MSV3drs760010175
GWAS Ctlgrs760010175
Max Magnitude0
ClinVar
Risk rs760010175(A;A)
Alt rs760010175(A;A)
Reference rs760010175(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.39076589G>A
CLNSRC
CLNACC RCV000182612.1,