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rs121909326

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909326(C;C)
Make rs121909326(C;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position13235219
GeneCACNA1A
is asnp
is mentioned by
dbSNPrs121909326
ebirs121909326
HLIrs121909326
Exacrs121909326
Varsomers121909326
Maprs121909326
PheGenIrs121909326
hapmaprs121909326
1000 genomesrs121909326
hgdprs121909326
ensemblrs121909326
gopubmedrs121909326
geneviewrs121909326
scholarrs121909326
googlers121909326
pharmgkbrs121909326
gwascentralrs121909326
openSNPrs121909326
23andMers121909326
23andMe allrs121909326
SNP Nexus

SNPshotrs121909326
SNPdbers121909326
MSV3drs121909326
GWAS Ctlgrs121909326
Max Magnitude0
OMIM601011
Desc
Variant0024
Relatedalso
ClinVar
Risk rs121909326(C;C)
Alt rs121909326(C;C)
Reference rs121909326(T;T)
Significance Pathogenic
Disease Familial hemiplegic migraine type 1 Spinocerebellar ataxia 6 Episodic ataxia type 2
Variation info
Gene CACNA1A
CLNDBN Familial hemiplegic migraine type 1 Spinocerebellar ataxia 6 Episodic ataxia type 2
Reversed 1
HGVS NC_000019.9:g.13346033A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000009035.2, RCV000009036.2, RCV000157056.2,