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rs121918616

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918616(A;A)
Make rs121918616(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position160130283
GeneATP1A2
is asnp
is mentioned by
dbSNPrs121918616
ebirs121918616
HLIrs121918616
Exacrs121918616
Varsomers121918616
Maprs121918616
PheGenIrs121918616
hapmaprs121918616
1000 genomesrs121918616
hgdprs121918616
ensemblrs121918616
gopubmedrs121918616
geneviewrs121918616
scholarrs121918616
googlers121918616
pharmgkbrs121918616
gwascentralrs121918616
openSNPrs121918616
23andMers121918616
23andMe allrs121918616
SNP Nexus

SNPshotrs121918616
SNPdbers121918616
MSV3drs121918616
GWAS Ctlgrs121918616
Max Magnitude0
OMIM182340
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121918616(A;A)
Alt rs121918616(A;A)
Reference rs121918616(G;G)
Significance Pathogenic
Disease Migraine
Variation info
Gene ATP1A2
CLNDBN Migraine, familial basilar
Reversed 0
HGVS NC_000001.10:g.160100073G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013789.18,