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rs121909132

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909132(A;A)
Make rs121909132(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position16048537
GeneCLCNKA, CLCNKB
is asnp
is mentioned by
dbSNPrs121909132
ebirs121909132
HLIrs121909132
Exacrs121909132
Varsomers121909132
Maprs121909132
PheGenIrs121909132
hapmaprs121909132
1000 genomesrs121909132
hgdprs121909132
ensemblrs121909132
gopubmedrs121909132
geneviewrs121909132
scholarrs121909132
googlers121909132
pharmgkbrs121909132
gwascentralrs121909132
openSNPrs121909132
23andMers121909132
23andMe allrs121909132
SNP Nexus

SNPshotrs121909132
SNPdbers121909132
MSV3drs121909132
GWAS Ctlgrs121909132
Max Magnitude0
OMIM602023
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909132(A;A)
Alt rs121909132(A;A)
Reference rs121909132(G;G)
Significance Pathogenic
Disease Bartter syndrome type 3
Variation info
Gene CLCNKB
CLNDBN Bartter syndrome type 3
Reversed 0
HGVS NC_000001.10:g.16375032G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008030.2,