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rs17215437

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in complete genomics
Make rs17215437(A;A)
Make rs17215437(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position74457316
GeneKCNE3
is asnp
is mentioned by
dbSNPrs17215437
dbSNP (classic)rs17215437
ClinGenrs17215437
ebirs17215437
HLIrs17215437
Exacrs17215437
Gnomadrs17215437
Varsomers17215437
LitVarrs17215437
Maprs17215437
PheGenIrs17215437
Biobankrs17215437
1000 genomesrs17215437
hgdprs17215437
ensemblrs17215437
geneviewrs17215437
scholarrs17215437
googlers17215437
pharmgkbrs17215437
gwascentralrs17215437
openSNPrs17215437
23andMers17215437
SNPshotrs17215437
SNPdbers17215437
MSV3drs17215437
GWAS Ctlgrs17215437
GMAF0.001837
Max Magnitude0
OMIM604433
DescHYPOKALEMIC PERIODIC PARALYSIS
Variant0001
Relatedalso


ClinVar
Risk rs17215437(A;A)
Alt rs17215437(A;A)
Reference Rs17215437(G;G)
Significance Other
Disease not provided Periodic paralysis not specified Cardiovascular phenotype Syncope Ventricular fibrillation
Variation info
Gene KCNE3
CLNDBN not provided Periodic paralysis not specified Cardiovascular phenotype Syncope Ventricular fibrillation
Reversed 1
HGVS NC_000011.9:g.74168361C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000005879.5, RCV000171813.1, RCV000223897.3, RCV000253742.1, RCV000415218.1,