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rs121908211

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908211(A;A)
Make rs121908211(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position13371744
GeneCACNA1A
is asnp
is mentioned by
dbSNPrs121908211
ebirs121908211
HLIrs121908211
Exacrs121908211
Varsomers121908211
Maprs121908211
PheGenIrs121908211
hapmaprs121908211
1000 genomesrs121908211
hgdprs121908211
ensemblrs121908211
gopubmedrs121908211
geneviewrs121908211
scholarrs121908211
googlers121908211
pharmgkbrs121908211
gwascentralrs121908211
openSNPrs121908211
23andMers121908211
23andMe allrs121908211
SNP Nexus

SNPshotrs121908211
SNPdbers121908211
MSV3drs121908211
GWAS Ctlgrs121908211
Merged fromRs121909310
Max Magnitude0
OMIM601011
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908211(A;A)
Alt rs121908211(A;A)
Reference rs121908211(G;G)
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.13482558C>T
CLNSRC OMIM Allelic Variant UniProtKB (variants)
CLNACC RCV000009008.3,