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rs28933398

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28933398(C;C)
Make rs28933398(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position160135845
GeneATP1A2
is asnp
is mentioned by
dbSNPrs28933398
ebirs28933398
HLIrs28933398
Exacrs28933398
Varsomers28933398
Maprs28933398
PheGenIrs28933398
hapmaprs28933398
1000 genomesrs28933398
hgdprs28933398
ensemblrs28933398
gopubmedrs28933398
geneviewrs28933398
scholarrs28933398
googlers28933398
pharmgkbrs28933398
gwascentralrs28933398
openSNPrs28933398
23andMers28933398
23andMe allrs28933398
SNP Nexus

SNPshotrs28933398
SNPdbers28933398
MSV3drs28933398
GWAS Ctlgrs28933398
Max Magnitude0
OMIM182340
DescMIGRAINE, FAMILIAL HEMIPLEGIC, 2
Variant0001
Relatedalso
Neighborrs28933400
Distance335
Neighborrs28933399
Distance820


ClinVar
Risk rs28933398(C;C)
Alt rs28933398(C;C)
Reference rs28933398(T;T)
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.160105635T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013780.25,