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rs750908017

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs750908017(A;C)
Make rs750908017(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237784139
GeneRYR2
is asnp
is mentioned by
dbSNPrs750908017
ebirs750908017
HLIrs750908017
Exacrs750908017
Varsomers750908017
Maprs750908017
PheGenIrs750908017
hapmaprs750908017
1000 genomesrs750908017
hgdprs750908017
ensemblrs750908017
gopubmedrs750908017
geneviewrs750908017
scholarrs750908017
googlers750908017
pharmgkbrs750908017
gwascentralrs750908017
openSNPrs750908017
23andMers750908017
23andMe allrs750908017
SNP Nexus

SNPshotrs750908017
SNPdbers750908017
MSV3drs750908017
GWAS Ctlgrs750908017
Max Magnitude0
ClinVar
Risk rs750908017(C,G;C,G)
Alt rs750908017(C,G;C,G)
Reference rs750908017(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947439A>C
CLNSRC
CLNACC RCV000182818.1,