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

rs606231441

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231441(A;A)
Make rs606231441(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position41970184
GeneATP1A3
is asnp
is mentioned by
dbSNPrs606231441
ebirs606231441
HLIrs606231441
Exacrs606231441
Varsomers606231441
Maprs606231441
PheGenIrs606231441
hapmaprs606231441
1000 genomesrs606231441
hgdprs606231441
ensemblrs606231441
gopubmedrs606231441
geneviewrs606231441
scholarrs606231441
googlers606231441
pharmgkbrs606231441
gwascentralrs606231441
openSNPrs606231441
23andMers606231441
23andMe allrs606231441
SNP Nexus

SNPshotrs606231441
SNPdbers606231441
MSV3drs606231441
GWAS Ctlgrs606231441
Max Magnitude0
ClinVar
Risk rs606231441(A;A)
Alt rs606231441(A;A)
Reference rs606231441(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.42474336C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000148326.1,