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rs1057520577

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520577(A;A)
Make rs1057520577(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position110333180
GeneATP2A2
is asnp
is mentioned by
dbSNPrs1057520577
dbSNP (old)rs1057520577
ClinGenrs1057520577
ebirs1057520577
HLIrs1057520577
Exacrs1057520577
Gnomadrs1057520577
Varsomers1057520577
Maprs1057520577
PheGenIrs1057520577
Biobankrs1057520577
1000 genomesrs1057520577
hgdprs1057520577
ensemblrs1057520577
gopubmedrs1057520577
geneviewrs1057520577
scholarrs1057520577
googlers1057520577
pharmgkbrs1057520577
gwascentralrs1057520577
openSNPrs1057520577
23andMers1057520577
23andMe allrs1057520577
SNPshotrs1057520577
SNPdbers1057520577
MSV3drs1057520577
GWAS Ctlgrs1057520577
Max Magnitude0
ClinVar
Risk rs1057520577(A;A)
Alt rs1057520577(A;A)
Reference Rs1057520577(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ATP2A2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.110770985G>A
CLNSRC
CLNACC RCV000444570.1,