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rs527236151

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236151(C;T)
Make rs527236151(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position21702913
GeneKCNJ18
is asnp
is mentioned by
dbSNPrs527236151
ebirs527236151
HLIrs527236151
Exacrs527236151
Varsomers527236151
Maprs527236151
PheGenIrs527236151
hapmaprs527236151
1000 genomesrs527236151
hgdprs527236151
ensemblrs527236151
gopubmedrs527236151
geneviewrs527236151
scholarrs527236151
googlers527236151
pharmgkbrs527236151
gwascentralrs527236151
openSNPrs527236151
23andMers527236151
23andMe allrs527236151
SNP Nexus

SNPshotrs527236151
SNPdbers527236151
MSV3drs527236151
GWAS Ctlgrs527236151
Max Magnitude0
ClinVar
Risk rs527236151(T;T)
Alt rs527236151(T;T)
Reference rs527236151(C;C)
Significance Pathogenic
Disease Thyrotoxic periodic paralysis
Variation info
Gene KCNJ18
CLNDBN Thyrotoxic periodic paralysis
Reversed 0
HGVS NC_000017.11:g.21702913C>T
CLNSRC ClinVar
CLNACC RCV000132738.2,