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rs199472817

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472817(A;G)
Make rs199472817(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2778036
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472817
ebirs199472817
HLIrs199472817
Exacrs199472817
Varsomers199472817
Maprs199472817
PheGenIrs199472817
hapmaprs199472817
1000 genomesrs199472817
hgdprs199472817
ensemblrs199472817
gopubmedrs199472817
geneviewrs199472817
scholarrs199472817
googlers199472817
pharmgkbrs199472817
gwascentralrs199472817
openSNPrs199472817
23andMers199472817
23andMe allrs199472817
SNP Nexus

SNPshotrs199472817
SNPdbers199472817
MSV3drs199472817
GWAS Ctlgrs199472817
Max Magnitude0
ClinVar
Risk rs199472817(G;G)
Alt rs199472817(G;G)
Reference rs199472817(A;A)
Significance Pathogenic
Disease SUDDEN INFANT DEATH SYNDROME
Variation info
Gene KCNQ1
CLNDBN SUDDEN INFANT DEATH SYNDROME
Reversed 0
HGVS NC_000011.9:g.2799266A>G
CLNSRC ClinVar
CLNACC RCV000057640.2,