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rs1057519173

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519173(A;A)
Make rs1057519173(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position38489444
GeneRYR1
is asnp
is mentioned by
dbSNPrs1057519173
dbSNP (old)rs1057519173
ClinGenrs1057519173
ebirs1057519173
HLIrs1057519173
Exacrs1057519173
Gnomadrs1057519173
Varsomers1057519173
LitVarrs1057519173
Maprs1057519173
PheGenIrs1057519173
Biobankrs1057519173
1000 genomesrs1057519173
hgdprs1057519173
ensemblrs1057519173
gopubmedrs1057519173
geneviewrs1057519173
scholarrs1057519173
googlers1057519173
pharmgkbrs1057519173
gwascentralrs1057519173
openSNPrs1057519173
23andMers1057519173
23andMe allrs1057519173
SNPshotrs1057519173
SNPdbers1057519173
MSV3drs1057519173
GWAS Ctlgrs1057519173
Max Magnitude0
ClinVar
Risk rs1057519173(A;A)
Alt rs1057519173(A;A)
Reference Rs1057519173(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.38980084G>A
CLNSRC
CLNACC RCV000416113.1,