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rs750349088

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs750349088(A;A)
Make rs750349088(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome21
Position34449373
GeneKCNE1
is asnp
is mentioned by
dbSNPrs750349088
dbSNP (classic)rs750349088
ClinGenrs750349088
ebirs750349088
HLIrs750349088
Exacrs750349088
Gnomadrs750349088
Varsomers750349088
LitVarrs750349088
Maprs750349088
PheGenIrs750349088
Biobankrs750349088
1000 genomesrs750349088
hgdprs750349088
ensemblrs750349088
geneviewrs750349088
scholarrs750349088
googlers750349088
pharmgkbrs750349088
gwascentralrs750349088
openSNPrs750349088
23andMers750349088
SNPshotrs750349088
SNPdbers750349088
MSV3drs750349088
GWAS Ctlgrs750349088
Max Magnitude0
ClinVar
Risk rs750349088(A;A) rs750349088(T;T)
Alt rs750349088(A;A) rs750349088(T;T)
Reference Rs750349088(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNE1B KCNE1
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.35821671G>A
CLNSRC
CLNACC RCV000256077.1,