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rs527236156

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236156(C;T)
Make rs527236156(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position21703981
GeneKCNJ18
is asnp
is mentioned by
dbSNPrs527236156
ebirs527236156
HLIrs527236156
Exacrs527236156
Varsomers527236156
Maprs527236156
PheGenIrs527236156
hapmaprs527236156
1000 genomesrs527236156
hgdprs527236156
ensemblrs527236156
gopubmedrs527236156
geneviewrs527236156
scholarrs527236156
googlers527236156
pharmgkbrs527236156
gwascentralrs527236156
openSNPrs527236156
23andMers527236156
23andMe allrs527236156
SNP Nexus

SNPshotrs527236156
SNPdbers527236156
MSV3drs527236156
GWAS Ctlgrs527236156
Max Magnitude0
ClinVar
Risk rs527236156(T;T)
Alt rs527236156(T;T)
Reference rs527236156(C;C)
Significance Pathogenic
Disease Thyrotoxic periodic paralysis
Variation info
Gene KCNJ18
CLNDBN Thyrotoxic periodic paralysis
Reversed 0
HGVS NC_000017.11:g.21703981C>T
CLNSRC ClinVar
CLNACC RCV000132743.2,