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rs1057518135

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518135(G;T)
Make rs1057518135(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position110322995
GeneATP2A2
is asnp
is mentioned by
dbSNPrs1057518135
dbSNP (old)rs1057518135
ClinGenrs1057518135
ebirs1057518135
HLIrs1057518135
Exacrs1057518135
Gnomadrs1057518135
Varsomers1057518135
Maprs1057518135
PheGenIrs1057518135
Biobankrs1057518135
1000 genomesrs1057518135
hgdprs1057518135
ensemblrs1057518135
gopubmedrs1057518135
geneviewrs1057518135
scholarrs1057518135
googlers1057518135
pharmgkbrs1057518135
gwascentralrs1057518135
openSNPrs1057518135
23andMers1057518135
23andMe allrs1057518135
SNPshotrs1057518135
SNPdbers1057518135
MSV3drs1057518135
GWAS Ctlgrs1057518135
Max Magnitude0
ClinVar
Risk rs1057518135(T;T)
Alt rs1057518135(T;T)
Reference Rs1057518135(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATP2A2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.110760800G>T
CLNSRC
CLNACC RCV000414184.1,