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rs28933400

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28933400(C;C)
Make rs28933400(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position160135510
GeneATP1A2
is asnp
is mentioned by
dbSNPrs28933400
ebirs28933400
HLIrs28933400
Exacrs28933400
Varsomers28933400
Maprs28933400
PheGenIrs28933400
hapmaprs28933400
1000 genomesrs28933400
hgdprs28933400
ensemblrs28933400
gopubmedrs28933400
geneviewrs28933400
scholarrs28933400
googlers28933400
pharmgkbrs28933400
gwascentralrs28933400
openSNPrs28933400
23andMers28933400
23andMe allrs28933400
SNP Nexus

SNPshotrs28933400
SNPdbers28933400
MSV3drs28933400
GWAS Ctlgrs28933400
Max Magnitude0
OMIM182340
DescMIGRAINE, FAMILIAL HEMIPLEGIC, 2
Variant0003
Relatedalso
Neighborrs28933401
Distance264
Neighborrs28933398
Distance335


ClinVar
Risk rs28933400(C;C)
Alt rs28933400(C;C)
Reference rs28933400(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.160105300T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013782.24,



[PMID 19199261] [Association of the polymorphisms of sodium transport related genes with essential hypertension].