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rs559626481

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs559626481(C;T)
Make rs559626481(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position56904401
GeneMIR6863, SLC12A3
is asnp
is mentioned by
dbSNPrs559626481
dbSNP (classic)rs559626481
ClinGenrs559626481
ebirs559626481
HLIrs559626481
Exacrs559626481
Gnomadrs559626481
Varsomers559626481
LitVarrs559626481
Maprs559626481
PheGenIrs559626481
Biobankrs559626481
1000 genomesrs559626481
hgdprs559626481
ensemblrs559626481
geneviewrs559626481
scholarrs559626481
googlers559626481
pharmgkbrs559626481
gwascentralrs559626481
openSNPrs559626481
23andMers559626481
23andMe allrs559626481
SNPshotrs559626481
SNPdbers559626481
MSV3drs559626481
GWAS Ctlgrs559626481
Max Magnitude0
ClinVar
Risk rs559626481(T;T)
Alt rs559626481(T;T)
Reference Rs559626481(C;C)
Significance Probable-Pathogenic
Disease Familial hypokalemia-hypomagnesemia
Variation info
Gene SLC12A3 MIR6863
CLNDBN Familial hypokalemia-hypomagnesemia
Reversed 0
HGVS NC_000016.9:g.56938313C>T
CLNSRC Illumina
CLNACC RCV000341379.1,