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rs863224858

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224858(-;-)
Make rs863224858(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position16055726
GeneCLCNKB
is asnp
is mentioned by
dbSNPrs863224858
dbSNP (old)rs863224858
ClinGenrs863224858
ebirs863224858
HLIrs863224858
Exacrs863224858
Gnomadrs863224858
Varsomers863224858
Maprs863224858
PheGenIrs863224858
Biobankrs863224858
1000 genomesrs863224858
hgdprs863224858
ensemblrs863224858
gopubmedrs863224858
geneviewrs863224858
scholarrs863224858
googlers863224858
pharmgkbrs863224858
gwascentralrs863224858
openSNPrs863224858
23andMers863224858
23andMe allrs863224858
SNP Nexus

SNPshotrs863224858
SNPdbers863224858
MSV3drs863224858
GWAS Ctlgrs863224858
Max Magnitude0
ClinVar
Risk rs863224858(-;-)
Alt rs863224858(-;-)
Reference Rs863224858(C;C)
Significance Probable-Pathogenic
Disease Bartter syndrome type 3
Variation info
Gene CLCNKB
CLNDBN Bartter syndrome type 3
Reversed 0
HGVS NC_000001.10:g.16382221delC
CLNSRC
CLNACC RCV000198263.1,