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rs36210419

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs36210419(A;G)
Make rs36210419(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2571372
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs36210419
ebirs36210419
HLIrs36210419
Exacrs36210419
Varsomers36210419
Maprs36210419
PheGenIrs36210419
hapmaprs36210419
1000 genomesrs36210419
hgdprs36210419
ensemblrs36210419
gopubmedrs36210419
geneviewrs36210419
scholarrs36210419
googlers36210419
pharmgkbrs36210419
gwascentralrs36210419
openSNPrs36210419
23andMers36210419
23andMe allrs36210419
SNP Nexus

SNPshotrs36210419
SNPdbers36210419
MSV3drs36210419
GWAS Ctlgrs36210419
Max Magnitude0


ClinVar
Risk rs36210419(G;G)
Alt rs36210419(G;G)
Reference rs36210419(A;A)
Significance Pathogenic
Disease Torsades de pointes not provided
Variation info
Gene KCNQ1
CLNDBN Torsades de pointes not provided
Reversed 0
HGVS NC_000011.9:g.2592602A>G
CLNSRC ClinVar
CLNACC RCV000057728.2, RCV000182096.2,