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rs527236153

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236153(-;-)
Make rs527236153(-;C)
ReferenceGRCh38 38.1/142
Chromosome17
Position21703215
GeneKCNJ18
is asnp
is mentioned by
dbSNPrs527236153
ebirs527236153
HLIrs527236153
Exacrs527236153
Varsomers527236153
Maprs527236153
PheGenIrs527236153
hapmaprs527236153
1000 genomesrs527236153
hgdprs527236153
ensemblrs527236153
gopubmedrs527236153
geneviewrs527236153
scholarrs527236153
googlers527236153
pharmgkbrs527236153
gwascentralrs527236153
openSNPrs527236153
23andMers527236153
23andMe allrs527236153
SNP Nexus

SNPshotrs527236153
SNPdbers527236153
MSV3drs527236153
GWAS Ctlgrs527236153
Max Magnitude0
ClinVar
Risk rs527236153(;)
Alt rs527236153(;)
Reference rs527236153(C;C)
Significance Pathogenic
Disease Thyrotoxic periodic paralysis
Variation info
Gene KCNJ18
CLNDBN Thyrotoxic periodic paralysis
Reversed 0
HGVS NC_000017.11:g.21703215delC
CLNSRC ClinVar
CLNACC RCV000132740.2,