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rs527236155

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236155(C;C)
Make rs527236155(C;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position21703384
GeneKCNJ18
is asnp
is mentioned by
dbSNPrs527236155
ebirs527236155
HLIrs527236155
Exacrs527236155
Varsomers527236155
Maprs527236155
PheGenIrs527236155
hapmaprs527236155
1000 genomesrs527236155
hgdprs527236155
ensemblrs527236155
gopubmedrs527236155
geneviewrs527236155
scholarrs527236155
googlers527236155
pharmgkbrs527236155
gwascentralrs527236155
openSNPrs527236155
23andMers527236155
23andMe allrs527236155
SNP Nexus

SNPshotrs527236155
SNPdbers527236155
MSV3drs527236155
GWAS Ctlgrs527236155
Max Magnitude0
ClinVar
Risk rs527236155(C;C)
Alt rs527236155(C;C)
Reference rs527236155(G;G)
Significance Pathogenic
Disease Thyrotoxic periodic paralysis
Variation info
Gene KCNJ18
CLNDBN Thyrotoxic periodic paralysis
Reversed 0
HGVS NC_000017.11:g.21703384G>C
CLNSRC ClinVar
CLNACC RCV000132742.2,