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rs17857111

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17857111(C;T)
Make rs17857111(T;T)
ReferenceGRCh38 38.1/142
Chromosome21
Position34449540
GeneKCNE1
is asnp
is mentioned by
dbSNPrs17857111
ClinGenrs17857111
ebirs17857111
HLIrs17857111
Exacrs17857111
Varsomers17857111
Maprs17857111
PheGenIrs17857111
hapmaprs17857111
1000 genomesrs17857111
hgdprs17857111
ensemblrs17857111
gopubmedrs17857111
geneviewrs17857111
scholarrs17857111
googlers17857111
pharmgkbrs17857111
gwascentralrs17857111
openSNPrs17857111
23andMers17857111
23andMe allrs17857111
SNP Nexus

SNPshotrs17857111
SNPdbers17857111
MSV3drs17857111
GWAS Ctlgrs17857111
Max Magnitude0
ClinVar
Risk rs17857111(T;T)
Alt rs17857111(T;T)
Reference Rs17857111(C;C)
Significance Untested
Disease Congenital long QT syndrome
Variation info
Gene KCNE1B KCNE1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000021.8:g.35821838C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000119095.2,