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rs121918619

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918619(C;T)
Make rs121918619(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position160123228
GeneATP1A2
is asnp
is mentioned by
dbSNPrs121918619
ebirs121918619
HLIrs121918619
Exacrs121918619
Varsomers121918619
Maprs121918619
PheGenIrs121918619
hapmaprs121918619
1000 genomesrs121918619
hgdprs121918619
ensemblrs121918619
gopubmedrs121918619
geneviewrs121918619
scholarrs121918619
googlers121918619
pharmgkbrs121918619
gwascentralrs121918619
openSNPrs121918619
23andMers121918619
23andMe allrs121918619
SNP Nexus

SNPshotrs121918619
SNPdbers121918619
MSV3drs121918619
GWAS Ctlgrs121918619
Max Magnitude0
OMIM182340
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121918619(T;T)
Alt rs121918619(T;T)
Reference rs121918619(C;C)
Significance Pathogenic
Disease Familial hemiplegic migraine type 2
Variation info
Gene ATP1A2
CLNDBN Familial hemiplegic migraine type 2
Reversed 0
HGVS NC_000001.10:g.160093018C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013792.24,