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rs121909136

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909136(A;A)
Make rs121909136(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position16055508
GeneCLCNKA, CLCNKB
is asnp
is mentioned by
dbSNPrs121909136
ebirs121909136
HLIrs121909136
Exacrs121909136
Varsomers121909136
Maprs121909136
PheGenIrs121909136
hapmaprs121909136
1000 genomesrs121909136
hgdprs121909136
ensemblrs121909136
gopubmedrs121909136
geneviewrs121909136
scholarrs121909136
googlers121909136
pharmgkbrs121909136
gwascentralrs121909136
openSNPrs121909136
23andMers121909136
23andMe allrs121909136
SNP Nexus

SNPshotrs121909136
SNPdbers121909136
MSV3drs121909136
GWAS Ctlgrs121909136
Max Magnitude0
OMIM602023
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121909136(A;A)
Alt rs121909136(A;A)
Reference rs121909136(G;G)
Significance Pathogenic
Disease Bartter syndrome
Variation info
Gene CLCNKB
CLNDBN Bartter syndrome, type 3, with hypocalciuria
Reversed 0
HGVS NC_000001.10:g.16382003G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008037.3,