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rs571985775

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs571985775(A;A)
Make rs571985775(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237785999
GeneRYR2
is asnp
is mentioned by
dbSNPrs571985775
ebirs571985775
HLIrs571985775
Exacrs571985775
Varsomers571985775
Maprs571985775
PheGenIrs571985775
hapmaprs571985775
1000 genomesrs571985775
hgdprs571985775
ensemblrs571985775
gopubmedrs571985775
geneviewrs571985775
scholarrs571985775
googlers571985775
pharmgkbrs571985775
gwascentralrs571985775
openSNPrs571985775
23andMers571985775
23andMe allrs571985775
SNP Nexus

SNPshotrs571985775
SNPdbers571985775
MSV3drs571985775
GWAS Ctlgrs571985775
Max Magnitude0
ClinVar
Risk rs571985775(A;A)
Alt rs571985775(A;A)
Reference rs571985775(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene RYR2
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.237949299G>A
CLNSRC
CLNACC RCV000151775.4,