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rs199472811

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472811(A;A)
Make rs199472811(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2777993
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472811
ebirs199472811
HLIrs199472811
Exacrs199472811
Varsomers199472811
Maprs199472811
PheGenIrs199472811
hapmaprs199472811
1000 genomesrs199472811
hgdprs199472811
ensemblrs199472811
gopubmedrs199472811
geneviewrs199472811
scholarrs199472811
googlers199472811
pharmgkbrs199472811
gwascentralrs199472811
openSNPrs199472811
23andMers199472811
23andMe allrs199472811
SNP Nexus

SNPshotrs199472811
SNPdbers199472811
MSV3drs199472811
GWAS Ctlgrs199472811
Max Magnitude0
ClinVar
Risk rs199472811(A;A)
Alt rs199472811(A;A)
Reference rs199472811(G;G)
Significance Pathogenic
Disease SUDDEN INFANT DEATH SYNDROME
Variation info
Gene KCNQ1
CLNDBN SUDDEN INFANT DEATH SYNDROME
Reversed 0
HGVS NC_000011.9:g.2799223G>A
CLNSRC ClinVar
CLNACC RCV000057630.2,