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rs1057516207

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057516207(-;A)
Make rs1057516207(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position16051793
GeneCLCNKB
is asnp
is mentioned by
dbSNPrs1057516207
dbSNP (old)rs1057516207
ClinGenrs1057516207
ebirs1057516207
HLIrs1057516207
Exacrs1057516207
Gnomadrs1057516207
Varsomers1057516207
Maprs1057516207
PheGenIrs1057516207
Biobankrs1057516207
1000 genomesrs1057516207
hgdprs1057516207
ensemblrs1057516207
gopubmedrs1057516207
geneviewrs1057516207
scholarrs1057516207
googlers1057516207
pharmgkbrs1057516207
gwascentralrs1057516207
openSNPrs1057516207
23andMers1057516207
23andMe allrs1057516207
SNPshotrs1057516207
SNPdbers1057516207
MSV3drs1057516207
GWAS Ctlgrs1057516207
Max Magnitude0
ClinVar
Risk rs1057516207(A;A)
Alt rs1057516207(A;A)
Reference Rs1057516207(-;-)
Significance Pathogenic
Disease Bartter syndrome type 3
Variation info
Gene CLCNKB
CLNDBN Bartter syndrome type 3
Reversed 0
HGVS NC_000001.10:g.16378288dupA
CLNSRC
CLNACC RCV000408763.1,