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rs1057521630

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521630(G;T)
Make rs1057521630(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position160128656
GeneATP1A2
is asnp
is mentioned by
dbSNPrs1057521630
dbSNP (old)rs1057521630
ClinGenrs1057521630
ebirs1057521630
HLIrs1057521630
Exacrs1057521630
Gnomadrs1057521630
Varsomers1057521630
Maprs1057521630
PheGenIrs1057521630
Biobankrs1057521630
1000 genomesrs1057521630
hgdprs1057521630
ensemblrs1057521630
gopubmedrs1057521630
geneviewrs1057521630
scholarrs1057521630
googlers1057521630
pharmgkbrs1057521630
gwascentralrs1057521630
openSNPrs1057521630
23andMers1057521630
23andMe allrs1057521630
SNPshotrs1057521630
SNPdbers1057521630
MSV3drs1057521630
GWAS Ctlgrs1057521630
Max Magnitude0
ClinVar
Risk rs1057521630(T;T)
Alt rs1057521630(T;T)
Reference Rs1057521630(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATP1A2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.160098446G>T
CLNSRC
CLNACC RCV000443567.1,