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rs1057523844

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523844(G;T)
Make rs1057523844(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position38506547
GeneRYR1
is asnp
is mentioned by
dbSNPrs1057523844
dbSNP (old)rs1057523844
ClinGenrs1057523844
ebirs1057523844
HLIrs1057523844
Exacrs1057523844
Gnomadrs1057523844
Varsomers1057523844
Maprs1057523844
PheGenIrs1057523844
Biobankrs1057523844
1000 genomesrs1057523844
hgdprs1057523844
ensemblrs1057523844
gopubmedrs1057523844
geneviewrs1057523844
scholarrs1057523844
googlers1057523844
pharmgkbrs1057523844
gwascentralrs1057523844
openSNPrs1057523844
23andMers1057523844
23andMe allrs1057523844
SNPshotrs1057523844
SNPdbers1057523844
MSV3drs1057523844
GWAS Ctlgrs1057523844
Max Magnitude0
ClinVar
Risk rs1057523844(T;T)
Alt rs1057523844(T;T)
Reference Rs1057523844(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.38997187G>T
CLNSRC
CLNACC RCV000440510.1,