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rs527236157

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236157(C;T)
Make rs527236157(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position21704005
GeneKCNJ18
is asnp
is mentioned by
dbSNPrs527236157
ebirs527236157
HLIrs527236157
Exacrs527236157
Varsomers527236157
Maprs527236157
PheGenIrs527236157
hapmaprs527236157
1000 genomesrs527236157
hgdprs527236157
ensemblrs527236157
gopubmedrs527236157
geneviewrs527236157
scholarrs527236157
googlers527236157
pharmgkbrs527236157
gwascentralrs527236157
openSNPrs527236157
23andMers527236157
23andMe allrs527236157
SNP Nexus

SNPshotrs527236157
SNPdbers527236157
MSV3drs527236157
GWAS Ctlgrs527236157
Max Magnitude0
ClinVar
Risk rs527236157(T;T)
Alt rs527236157(T;T)
Reference rs527236157(C;C)
Significance Pathogenic
Disease Thyrotoxic periodic paralysis
Variation info
Gene KCNJ18
CLNDBN Thyrotoxic periodic paralysis
Reversed 0
HGVS NC_000017.11:g.21704005C>T
CLNSRC ClinVar
CLNACC RCV000132744.2,