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rs121918618

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918618(C;T)
Make rs121918618(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position160129007
GeneATP1A2
is asnp
is mentioned by
dbSNPrs121918618
ebirs121918618
HLIrs121918618
Exacrs121918618
Varsomers121918618
Maprs121918618
PheGenIrs121918618
hapmaprs121918618
1000 genomesrs121918618
hgdprs121918618
ensemblrs121918618
gopubmedrs121918618
geneviewrs121918618
scholarrs121918618
googlers121918618
pharmgkbrs121918618
gwascentralrs121918618
openSNPrs121918618
23andMers121918618
23andMe allrs121918618
SNP Nexus

SNPshotrs121918618
SNPdbers121918618
MSV3drs121918618
GWAS Ctlgrs121918618
Max Magnitude0
OMIM182340
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121918618(T;T)
Alt rs121918618(T;T)
Reference rs121918618(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.160098797C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013791.26,