Have questions? Visit https://www.reddit.com/r/SNPedia

rs121918620

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918620(C;T)
Make rs121918620(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position160128761
GeneATP1A2
is asnp
is mentioned by
dbSNPrs121918620
ebirs121918620
HLIrs121918620
Exacrs121918620
Varsomers121918620
Maprs121918620
PheGenIrs121918620
hapmaprs121918620
1000 genomesrs121918620
hgdprs121918620
ensemblrs121918620
gopubmedrs121918620
geneviewrs121918620
scholarrs121918620
googlers121918620
pharmgkbrs121918620
gwascentralrs121918620
openSNPrs121918620
23andMers121918620
23andMe allrs121918620
SNP Nexus

SNPshotrs121918620
SNPdbers121918620
MSV3drs121918620
GWAS Ctlgrs121918620
Max Magnitude0
OMIM182340
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121918620(T;T)
Alt rs121918620(T;T)
Reference rs121918620(C;C)
Significance Pathogenic
Disease not provided Familial hemiplegic migraine type 2
Variation info
Gene ATP1A2
CLNDBN not provided Familial hemiplegic migraine type 2
Reversed 0
HGVS NC_000001.10:g.160098551C>G; NC_000001.10:g.160098551C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000186787.1, RCV000013793.25,