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rs267607051

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607051(A;A)
Make rs267607051(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position56894594
GeneSLC12A3
is asnp
is mentioned by
dbSNPrs267607051
ebirs267607051
HLIrs267607051
Exacrs267607051
Varsomers267607051
Maprs267607051
PheGenIrs267607051
hapmaprs267607051
1000 genomesrs267607051
hgdprs267607051
ensemblrs267607051
gopubmedrs267607051
geneviewrs267607051
scholarrs267607051
googlers267607051
pharmgkbrs267607051
gwascentralrs267607051
openSNPrs267607051
23andMers267607051
23andMe allrs267607051
SNP Nexus

SNPshotrs267607051
SNPdbers267607051
MSV3drs267607051
GWAS Ctlgrs267607051
Max Magnitude0
ClinVar
Risk rs267607051(A;A)
Alt rs267607051(A;A)
Reference rs267607051(G;G)
Significance Pathogenic
Disease Familial hypokalemia-hypomagnesemia
Variation info
Gene SLC12A3
CLNDBN Familial hypokalemia-hypomagnesemia
Reversed 0
HGVS NC_000016.9:g.56928506G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009127.3,