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rs202114767

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202114767(A;A)
Make rs202114767(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position56904402
GeneMIR6863, SLC12A3
is asnp
is mentioned by
dbSNPrs202114767
dbSNP (classic)rs202114767
ClinGenrs202114767
ebirs202114767
HLIrs202114767
Exacrs202114767
Gnomadrs202114767
Varsomers202114767
LitVarrs202114767
Maprs202114767
PheGenIrs202114767
Biobankrs202114767
1000 genomesrs202114767
hgdprs202114767
ensemblrs202114767
geneviewrs202114767
scholarrs202114767
googlers202114767
pharmgkbrs202114767
gwascentralrs202114767
openSNPrs202114767
23andMers202114767
23andMe allrs202114767
SNPshotrs202114767
SNPdbers202114767
MSV3drs202114767
GWAS Ctlgrs202114767
Max Magnitude0
ClinVar
Risk rs202114767(A;A)
Alt rs202114767(A;A)
Reference Rs202114767(G;G)
Significance Pathogenic
Disease Familial hypokalemia-hypomagnesemia
Variation info
Gene SLC12A3 MIR6863
CLNDBN Familial hypokalemia-hypomagnesemia
Reversed 0
HGVS NC_000016.9:g.56938314G>A
CLNSRC
CLNACC RCV000477802.1,