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rs121918617

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121918617(C;C)
Make rs121918617(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position160127660
GeneATP1A2
is asnp
is mentioned by
dbSNPrs121918617
ebirs121918617
HLIrs121918617
Exacrs121918617
Varsomers121918617
Maprs121918617
PheGenIrs121918617
hapmaprs121918617
1000 genomesrs121918617
hgdprs121918617
ensemblrs121918617
gopubmedrs121918617
geneviewrs121918617
scholarrs121918617
googlers121918617
pharmgkbrs121918617
gwascentralrs121918617
openSNPrs121918617
23andMers121918617
23andMe allrs121918617
SNP Nexus

SNPshotrs121918617
SNPdbers121918617
MSV3drs121918617
GWAS Ctlgrs121918617
Max Magnitude0
OMIM182340
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121918617(C;C)
Alt rs121918617(C;C)
Reference rs121918617(T;T)
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.160097450T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013790.26,