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rs121918615

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918615(C;T)
Make rs121918615(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position160139735
GeneATP1A2
is asnp
is mentioned by
dbSNPrs121918615
ebirs121918615
HLIrs121918615
Exacrs121918615
Varsomers121918615
Maprs121918615
PheGenIrs121918615
hapmaprs121918615
1000 genomesrs121918615
hgdprs121918615
ensemblrs121918615
gopubmedrs121918615
geneviewrs121918615
scholarrs121918615
googlers121918615
pharmgkbrs121918615
gwascentralrs121918615
openSNPrs121918615
23andMers121918615
23andMe allrs121918615
SNP Nexus

SNPshotrs121918615
SNPdbers121918615
MSV3drs121918615
GWAS Ctlgrs121918615
Max Magnitude0
OMIM182340
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121918615(T;T)
Alt rs121918615(T;T)
Reference rs121918615(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.160109525C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013788.26,