Have questions? Visit https://www.reddit.com/r/SNPedia

rs606231430

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231430(G;T)
Make rs606231430(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position41982102
GeneATP1A3
is asnp
is mentioned by
dbSNPrs606231430
ebirs606231430
HLIrs606231430
Exacrs606231430
Varsomers606231430
Maprs606231430
PheGenIrs606231430
hapmaprs606231430
1000 genomesrs606231430
hgdprs606231430
ensemblrs606231430
gopubmedrs606231430
geneviewrs606231430
scholarrs606231430
googlers606231430
pharmgkbrs606231430
gwascentralrs606231430
openSNPrs606231430
23andMers606231430
23andMe allrs606231430
SNP Nexus

SNPshotrs606231430
SNPdbers606231430
MSV3drs606231430
GWAS Ctlgrs606231430
Max Magnitude0
ClinVar
Risk rs606231430(T;T)
Alt rs606231430(T;T)
Reference rs606231430(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.42486254C>A
CLNSRC
CLNACC RCV000148308.1,