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rs397508121

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508121(-;-)
Make rs397508121(-;GT)
Make rs397508121(GT;GT)
ReferenceGRCh38 38.1/141
Chromosome11
Position2571384
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508121
ebirs397508121
HLIrs397508121
Exacrs397508121
Varsomers397508121
Maprs397508121
PheGenIrs397508121
hapmaprs397508121
1000 genomesrs397508121
hgdprs397508121
ensemblrs397508121
gopubmedrs397508121
geneviewrs397508121
scholarrs397508121
googlers397508121
pharmgkbrs397508121
gwascentralrs397508121
openSNPrs397508121
23andMers397508121
23andMe allrs397508121
SNP Nexus

SNPshotrs397508121
SNPdbers397508121
MSV3drs397508121
GWAS Ctlgrs397508121
Max Magnitude0
ClinVar
Risk rs397508121(GT;GT)
Alt rs397508121(GT;GT)
Reference rs397508121(;)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2592613_2592614dupGT
CLNSRC ClinVar
CLNACC RCV000046102.2,