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rs794728557

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGGTGGTAAGTC;GGGTGGTAAGTC) 0 common in clinvar
Make rs794728557(-;-)
Make rs794728557(-;GTGGTAAGTCGG)
Make rs794728557(GTGGTAAGTCGG;GTGGTAAGTCGG)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2572984
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728557
dbSNP (old)rs794728557
ClinGenrs794728557
ebirs794728557
HLIrs794728557
Exacrs794728557
Gnomadrs794728557
Varsomers794728557
Maprs794728557
PheGenIrs794728557
Biobankrs794728557
1000 genomesrs794728557
hgdprs794728557
ensemblrs794728557
gopubmedrs794728557
geneviewrs794728557
scholarrs794728557
googlers794728557
pharmgkbrs794728557
gwascentralrs794728557
openSNPrs794728557
23andMers794728557
23andMe allrs794728557
SNP Nexus

SNPshotrs794728557
SNPdbers794728557
MSV3drs794728557
GWAS Ctlgrs794728557
Max Magnitude0
ClinVar
Risk rs794728557(-;-)
Alt rs794728557(-;-)
Reference Rs794728557(GGGTGGTAAGTC;GGGTGGTAAGTC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2594214_2594225delGTGGTAAGTCGG
CLNSRC
CLNACC RCV000182272.2,