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rs606231445

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231445(C;G)
Make rs606231445(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position41968823
GeneATP1A3
is asnp
is mentioned by
dbSNPrs606231445
ebirs606231445
HLIrs606231445
Exacrs606231445
Varsomers606231445
Maprs606231445
PheGenIrs606231445
hapmaprs606231445
1000 genomesrs606231445
hgdprs606231445
ensemblrs606231445
gopubmedrs606231445
geneviewrs606231445
scholarrs606231445
googlers606231445
pharmgkbrs606231445
gwascentralrs606231445
openSNPrs606231445
23andMers606231445
23andMe allrs606231445
SNP Nexus

SNPshotrs606231445
SNPdbers606231445
MSV3drs606231445
GWAS Ctlgrs606231445
Max Magnitude0
ClinVar
Risk rs606231445(G,T;G,T)
Alt rs606231445(G,T;G,T)
Reference rs606231445(C;C)
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.42472975G>C
CLNSRC
CLNACC RCV000148332.1,