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rs606231432

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231432(G;T)
Make rs606231432(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position41982028
GeneATP1A3
is asnp
is mentioned by
dbSNPrs606231432
ebirs606231432
HLIrs606231432
Exacrs606231432
Varsomers606231432
Maprs606231432
PheGenIrs606231432
hapmaprs606231432
1000 genomesrs606231432
hgdprs606231432
ensemblrs606231432
gopubmedrs606231432
geneviewrs606231432
scholarrs606231432
googlers606231432
pharmgkbrs606231432
gwascentralrs606231432
openSNPrs606231432
23andMers606231432
23andMe allrs606231432
SNP Nexus

SNPshotrs606231432
SNPdbers606231432
MSV3drs606231432
GWAS Ctlgrs606231432
Max Magnitude0
ClinVar
Risk rs606231432(T;T)
Alt rs606231432(T;T)
Reference rs606231432(G;G)
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.42486180C>A
CLNSRC
CLNACC RCV000148310.1,