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rs606231427

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs606231427(A;T)
Make rs606231427(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position41986168
GeneATP1A3
is asnp
is mentioned by
dbSNPrs606231427
ebirs606231427
HLIrs606231427
Exacrs606231427
Varsomers606231427
Maprs606231427
PheGenIrs606231427
hapmaprs606231427
1000 genomesrs606231427
hgdprs606231427
ensemblrs606231427
gopubmedrs606231427
geneviewrs606231427
scholarrs606231427
googlers606231427
pharmgkbrs606231427
gwascentralrs606231427
openSNPrs606231427
23andMers606231427
23andMe allrs606231427
SNP Nexus

SNPshotrs606231427
SNPdbers606231427
MSV3drs606231427
GWAS Ctlgrs606231427
Max Magnitude0
ClinVar
Risk rs606231427(T;T)
Alt rs606231427(T;T)
Reference rs606231427(A;A)
Significance Pathogenic
Disease Alternating hemiplegia of childhood 2
Variation info
Gene ATP1A3
CLNDBN Alternating hemiplegia of childhood 2
Reversed 1
HGVS NC_000019.9:g.42490320T>A
CLNSRC
CLNACC RCV000148304.1,