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rs121918612

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918612(A;A)
Make rs121918612(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position160127704
GeneATP1A2
is asnp
is mentioned by
dbSNPrs121918612
ebirs121918612
HLIrs121918612
Exacrs121918612
Varsomers121918612
Maprs121918612
PheGenIrs121918612
hapmaprs121918612
1000 genomesrs121918612
hgdprs121918612
ensemblrs121918612
gopubmedrs121918612
geneviewrs121918612
scholarrs121918612
googlers121918612
pharmgkbrs121918612
gwascentralrs121918612
openSNPrs121918612
23andMers121918612
23andMe allrs121918612
SNP Nexus

SNPshotrs121918612
SNPdbers121918612
MSV3drs121918612
GWAS Ctlgrs121918612
Max Magnitude0
OMIM182340
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121918612(A;A)
Alt rs121918612(A;A)
Reference rs121918612(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.160097494G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013785.25,