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rs797044897

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044897(A;G)
Make rs797044897(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position41984940
GeneATP1A3
is asnp
is mentioned by
dbSNPrs797044897
ebirs797044897
HLIrs797044897
Exacrs797044897
Varsomers797044897
Maprs797044897
PheGenIrs797044897
hapmaprs797044897
1000 genomesrs797044897
hgdprs797044897
ensemblrs797044897
gopubmedrs797044897
geneviewrs797044897
scholarrs797044897
googlers797044897
pharmgkbrs797044897
gwascentralrs797044897
openSNPrs797044897
23andMers797044897
23andMe allrs797044897
SNP Nexus

SNPshotrs797044897
SNPdbers797044897
MSV3drs797044897
GWAS Ctlgrs797044897
Max Magnitude0
ClinVar
Risk rs797044897(G;G)
Alt rs797044897(G;G)
Reference rs797044897(A;A)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ATP1A3
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000019.9:g.42489092T>C
CLNSRC
CLNACC RCV000190721.1,