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rs121918614

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918614(A;A)
Make rs121918614(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position160135470
GeneATP1A2
is asnp
is mentioned by
dbSNPrs121918614
ebirs121918614
HLIrs121918614
Exacrs121918614
Varsomers121918614
Maprs121918614
PheGenIrs121918614
hapmaprs121918614
1000 genomesrs121918614
hgdprs121918614
ensemblrs121918614
gopubmedrs121918614
geneviewrs121918614
scholarrs121918614
googlers121918614
pharmgkbrs121918614
gwascentralrs121918614
openSNPrs121918614
23andMers121918614
23andMe allrs121918614
SNP Nexus

SNPshotrs121918614
SNPdbers121918614
MSV3drs121918614
GWAS Ctlgrs121918614
Max Magnitude0
OMIM182340
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121918614(A;A)
Alt rs121918614(A;A)
Reference rs121918614(G;G)
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.160105260G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013787.25,