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rs747321794

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs747321794(A;A)
Make rs747321794(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position34449462
GeneKCNE1
is asnp
is mentioned by
dbSNPrs747321794
dbSNP (classic)rs747321794
ClinGenrs747321794
ebirs747321794
HLIrs747321794
Exacrs747321794
Gnomadrs747321794
Varsomers747321794
LitVarrs747321794
Maprs747321794
PheGenIrs747321794
Biobankrs747321794
1000 genomesrs747321794
hgdprs747321794
ensemblrs747321794
geneviewrs747321794
scholarrs747321794
googlers747321794
pharmgkbrs747321794
gwascentralrs747321794
openSNPrs747321794
23andMers747321794
SNPshotrs747321794
SNPdbers747321794
MSV3drs747321794
GWAS Ctlgrs747321794
Max Magnitude0
ClinVar
Risk rs747321794(A;A)
Alt rs747321794(A;A)
Reference Rs747321794(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNE1B KCNE1
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.35821760G>A
CLNSRC
CLNACC RCV000414735.1,