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rs886039754

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs886039754(A;G)
Make rs886039754(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position56885358
GeneSLC12A3
is asnp
is mentioned by
dbSNPrs886039754
dbSNP (classic)rs886039754
ClinGenrs886039754
ebirs886039754
HLIrs886039754
Exacrs886039754
Gnomadrs886039754
Varsomers886039754
LitVarrs886039754
Maprs886039754
PheGenIrs886039754
Biobankrs886039754
1000 genomesrs886039754
hgdprs886039754
ensemblrs886039754
geneviewrs886039754
scholarrs886039754
googlers886039754
pharmgkbrs886039754
gwascentralrs886039754
openSNPrs886039754
23andMers886039754
23andMe allrs886039754
SNPshotrs886039754
SNPdbers886039754
MSV3drs886039754
GWAS Ctlgrs886039754
Max Magnitude0
ClinVar
Risk rs886039754(G;G)
Alt rs886039754(G;G)
Reference Rs886039754(A;A)
Significance Pathogenic
Disease Familial hypokalemia-hypomagnesemia
Variation info
Gene SLC12A3
CLNDBN Familial hypokalemia-hypomagnesemia
Reversed 0
HGVS NC_000016.9:g.56919270A>G
CLNSRC
CLNACC RCV000256196.1,