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rs121909135

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909135(C;C)
Make rs121909135(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position16051544
GeneCLCNKA, CLCNKB
is asnp
is mentioned by
dbSNPrs121909135
ebirs121909135
HLIrs121909135
Exacrs121909135
Varsomers121909135
Maprs121909135
PheGenIrs121909135
hapmaprs121909135
1000 genomesrs121909135
hgdprs121909135
ensemblrs121909135
gopubmedrs121909135
geneviewrs121909135
scholarrs121909135
googlers121909135
pharmgkbrs121909135
gwascentralrs121909135
openSNPrs121909135
23andMers121909135
23andMe allrs121909135
SNP Nexus

SNPshotrs121909135
SNPdbers121909135
MSV3drs121909135
GWAS Ctlgrs121909135
Max Magnitude0
OMIM602023
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909135(C;C)
Alt rs121909135(C;C)
Reference rs121909135(T;T)
Significance Pathogenic
Disease Bartter syndrome type 3
Variation info
Gene CLCNKB
CLNDBN Bartter syndrome type 3
Reversed 0
HGVS NC_000001.10:g.16378039T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008033.2,