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rs1057518457

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518457(A;C)
Make rs1057518457(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position110339501
GeneATP2A2
is asnp
is mentioned by
dbSNPrs1057518457
dbSNP (old)rs1057518457
ClinGenrs1057518457
ebirs1057518457
HLIrs1057518457
Exacrs1057518457
Gnomadrs1057518457
Varsomers1057518457
LitVarrs1057518457
Maprs1057518457
PheGenIrs1057518457
Biobankrs1057518457
1000 genomesrs1057518457
hgdprs1057518457
ensemblrs1057518457
gopubmedrs1057518457
geneviewrs1057518457
scholarrs1057518457
googlers1057518457
pharmgkbrs1057518457
gwascentralrs1057518457
openSNPrs1057518457
23andMers1057518457
23andMe allrs1057518457
SNPshotrs1057518457
SNPdbers1057518457
MSV3drs1057518457
GWAS Ctlgrs1057518457
Max Magnitude0
ClinVar
Risk rs1057518457(C;C)
Alt rs1057518457(C;C)
Reference Rs1057518457(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATP2A2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.110777306A>C
CLNSRC
CLNACC RCV000414137.1,