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rs864309572

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309572(C;T)
Make rs864309572(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position41984944
GeneATP1A3
is asnp
is mentioned by
dbSNPrs864309572
ebirs864309572
HLIrs864309572
Exacrs864309572
Varsomers864309572
Maprs864309572
PheGenIrs864309572
hapmaprs864309572
1000 genomesrs864309572
hgdprs864309572
ensemblrs864309572
gopubmedrs864309572
geneviewrs864309572
scholarrs864309572
googlers864309572
pharmgkbrs864309572
gwascentralrs864309572
openSNPrs864309572
23andMers864309572
23andMe allrs864309572
SNP Nexus

SNPshotrs864309572
SNPdbers864309572
MSV3drs864309572
GWAS Ctlgrs864309572
Max Magnitude0
ClinVar
Risk rs864309572(T;T)
Alt rs864309572(T;T)
Reference rs864309572(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ATP1A3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.42489096G>A
CLNSRC
CLNACC RCV000203207.1,