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rs794728555

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTC;TTC) 0 common in clinvar
Make rs794728555(-;-)
Make rs794728555(-;TTC)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2570649
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728555
dbSNP (old)rs794728555
ClinGenrs794728555
ebirs794728555
HLIrs794728555
Exacrs794728555
Gnomadrs794728555
Varsomers794728555
Maprs794728555
PheGenIrs794728555
Biobankrs794728555
1000 genomesrs794728555
hgdprs794728555
ensemblrs794728555
gopubmedrs794728555
geneviewrs794728555
scholarrs794728555
googlers794728555
pharmgkbrs794728555
gwascentralrs794728555
openSNPrs794728555
23andMers794728555
23andMe allrs794728555
SNP Nexus

SNPshotrs794728555
SNPdbers794728555
MSV3drs794728555
GWAS Ctlgrs794728555
Max Magnitude0
ClinVar
Risk rs794728555(-;-)
Alt rs794728555(-;-)
Reference Rs794728555(TTC;TTC)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNQ1
CLNDBN Cardiac arrhythmia
Reversed 0
HGVS NC_000011.9:g.2591879_2591881delTTC
CLNSRC
CLNACC RCV000182265.1,