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rs397515877

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515877(-;-)
Make rs397515877(-;ATCGCGCCC)
Make rs397515877(ATCGCGCCC;ATCGCGCCC)
ReferenceGRCh38 38.1/142
Chromosome11
Position2445266
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397515877
ebirs397515877
HLIrs397515877
Exacrs397515877
Varsomers397515877
Maprs397515877
PheGenIrs397515877
hapmaprs397515877
1000 genomesrs397515877
hgdprs397515877
ensemblrs397515877
gopubmedrs397515877
geneviewrs397515877
scholarrs397515877
googlers397515877
pharmgkbrs397515877
gwascentralrs397515877
openSNPrs397515877
23andMers397515877
23andMe allrs397515877
SNP Nexus

SNPshotrs397515877
SNPdbers397515877
MSV3drs397515877
GWAS Ctlgrs397515877
Max Magnitude0
ClinVar
Risk rs397515877(CGCGCCCAT;CGCGCCCAT)
Alt rs397515877(CGCGCCCAT;CGCGCCCAT)
Reference rs397515877(;)
Significance Other
Disease not specified Long QT syndrome Atrial fibrillation Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN not specified Long QT syndrome, LQT1 subtype Atrial fibrillation, familial, 3 Long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2466488_2466496dupATCGCGCCC
CLNSRC OMIM Allelic Variant
CLNACC RCV000035343.4, RCV000046005.2, RCV000114749.3, RCV000205136.1,