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rs527236154

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236154(A;A)
Make rs527236154(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position21703288
GeneKCNJ18
is asnp
is mentioned by
dbSNPrs527236154
ebirs527236154
HLIrs527236154
Exacrs527236154
Varsomers527236154
Maprs527236154
PheGenIrs527236154
hapmaprs527236154
1000 genomesrs527236154
hgdprs527236154
ensemblrs527236154
gopubmedrs527236154
geneviewrs527236154
scholarrs527236154
googlers527236154
pharmgkbrs527236154
gwascentralrs527236154
openSNPrs527236154
23andMers527236154
23andMe allrs527236154
SNP Nexus

SNPshotrs527236154
SNPdbers527236154
MSV3drs527236154
GWAS Ctlgrs527236154
Max Magnitude0
ClinVar
Risk rs527236154(A;A)
Alt rs527236154(A;A)
Reference rs527236154(G;G)
Significance Pathogenic
Disease Thyrotoxic periodic paralysis
Variation info
Gene KCNJ18
CLNDBN Thyrotoxic periodic paralysis
Reversed 0
HGVS NC_000017.11:g.21703288G>A
CLNSRC ClinVar
CLNACC RCV000132741.2,