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rs869025341

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025341(A;A)
Make rs869025341(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position160124371
GeneATP1A2
is asnp
is mentioned by
dbSNPrs869025341
ebirs869025341
HLIrs869025341
Exacrs869025341
Varsomers869025341
Maprs869025341
PheGenIrs869025341
hapmaprs869025341
1000 genomesrs869025341
hgdprs869025341
ensemblrs869025341
gopubmedrs869025341
geneviewrs869025341
scholarrs869025341
googlers869025341
pharmgkbrs869025341
gwascentralrs869025341
openSNPrs869025341
23andMers869025341
23andMe allrs869025341
SNP Nexus

SNPshotrs869025341
SNPdbers869025341
MSV3drs869025341
GWAS Ctlgrs869025341
Max Magnitude0
ClinVar
Risk rs869025341(A;A)
Alt rs869025341(A;A)
Reference rs869025341(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.160094161G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000207519.1,