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rs1057520789

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520789(A;G)
Make rs1057520789(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position110343297
GeneATP2A2
is asnp
is mentioned by
dbSNPrs1057520789
dbSNP (old)rs1057520789
ClinGenrs1057520789
ebirs1057520789
HLIrs1057520789
Exacrs1057520789
Gnomadrs1057520789
Varsomers1057520789
Maprs1057520789
PheGenIrs1057520789
Biobankrs1057520789
1000 genomesrs1057520789
hgdprs1057520789
ensemblrs1057520789
gopubmedrs1057520789
geneviewrs1057520789
scholarrs1057520789
googlers1057520789
pharmgkbrs1057520789
gwascentralrs1057520789
openSNPrs1057520789
23andMers1057520789
23andMe allrs1057520789
SNPshotrs1057520789
SNPdbers1057520789
MSV3drs1057520789
GWAS Ctlgrs1057520789
Max Magnitude0
ClinVar
Risk rs1057520789(G;G)
Alt rs1057520789(G;G)
Reference Rs1057520789(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ATP2A2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.110781102A>G
CLNSRC
CLNACC RCV000417773.1,