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rs121918613

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918613(A;G)
Make rs121918613(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position160128667
GeneATP1A2
is asnp
is mentioned by
dbSNPrs121918613
ebirs121918613
HLIrs121918613
Exacrs121918613
Varsomers121918613
Maprs121918613
PheGenIrs121918613
hapmaprs121918613
1000 genomesrs121918613
hgdprs121918613
ensemblrs121918613
gopubmedrs121918613
geneviewrs121918613
scholarrs121918613
googlers121918613
pharmgkbrs121918613
gwascentralrs121918613
openSNPrs121918613
23andMers121918613
23andMe allrs121918613
SNP Nexus

SNPshotrs121918613
SNPdbers121918613
MSV3drs121918613
GWAS Ctlgrs121918613
Max Magnitude0
OMIM182340
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121918613(G;G)
Alt rs121918613(G;G)
Reference rs121918613(A;A)
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.160098457A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013786.24,