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rs45610936

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs45610936(-;-)
Make rs45610936(-;CT)
ReferenceGRCh38.p2 38.2/144
Chromosome21
Position34370847
GeneKCNE2, LOC105372791
is asnp
is mentioned by
dbSNPrs45610936
dbSNP (classic)rs45610936
ClinGenrs45610936
ebirs45610936
HLIrs45610936
Exacrs45610936
Gnomadrs45610936
Varsomers45610936
LitVarrs45610936
Maprs45610936
PheGenIrs45610936
Biobankrs45610936
1000 genomesrs45610936
hgdprs45610936
ensemblrs45610936
geneviewrs45610936
scholarrs45610936
googlers45610936
pharmgkbrs45610936
gwascentralrs45610936
openSNPrs45610936
23andMers45610936
SNPshotrs45610936
SNPdbers45610936
MSV3drs45610936
GWAS Ctlgrs45610936
Max Magnitude0
ClinVar
Risk rs45610936(-;-)
Alt rs45610936(-;-)
Reference Rs45610936(CT;CT)
Significance Pathogenic
Disease not specified
Variation info
Gene KCNE2
CLNDBN not specified
Reversed 0
HGVS NC_000021.8:g.35743146_35743147delCT
CLNSRC
CLNACC RCV000170960.5,