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rs28933401

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28933401(A;A)
Make rs28933401(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position160135246
GeneATP1A2
is asnp
is mentioned by
dbSNPrs28933401
ebirs28933401
HLIrs28933401
Exacrs28933401
Varsomers28933401
Maprs28933401
PheGenIrs28933401
hapmaprs28933401
1000 genomesrs28933401
hgdprs28933401
ensemblrs28933401
gopubmedrs28933401
geneviewrs28933401
scholarrs28933401
googlers28933401
pharmgkbrs28933401
gwascentralrs28933401
openSNPrs28933401
23andMers28933401
23andMe allrs28933401
SNP Nexus

SNPshotrs28933401
SNPdbers28933401
MSV3drs28933401
GWAS Ctlgrs28933401
Max Magnitude0
OMIM182340
DescMIGRAINE, FAMILIAL HEMIPLEGIC, 2
Variant0004
Relatedalso
Neighborrs28933400
Distance264


ClinVar
Risk rs28933401(A;A)
Alt rs28933401(A;A)
Reference rs28933401(G;G)
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.160105036G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013783.19,