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rs121908213

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908213(C;C)
Make rs121908213(C;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position13303580
GeneCACNA1A
is asnp
is mentioned by
dbSNPrs121908213
ebirs121908213
HLIrs121908213
Exacrs121908213
Varsomers121908213
Maprs121908213
PheGenIrs121908213
hapmaprs121908213
1000 genomesrs121908213
hgdprs121908213
ensemblrs121908213
gopubmedrs121908213
geneviewrs121908213
scholarrs121908213
googlers121908213
pharmgkbrs121908213
gwascentralrs121908213
openSNPrs121908213
23andMers121908213
23andMe allrs121908213
SNP Nexus

SNPshotrs121908213
SNPdbers121908213
MSV3drs121908213
GWAS Ctlgrs121908213
Merged fromRs121909312
Max Magnitude0
OMIM601011
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908213(C;C)
Alt rs121908213(C;C)
Reference rs121908213(T;T)
Significance Pathogenic
Disease Familial hemiplegic migraine type 1
Variation info
Gene CACNA1A
CLNDBN Familial hemiplegic migraine type 1
Reversed 1
HGVS NC_000019.9:g.13414394A>G
CLNSRC OMIM Allelic Variant UniProtKB (variants)
CLNACC RCV000009011.4,