rs559626481

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs559626481(C;T)

Make rs559626481(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

56904401

Gene	MIR6863, SLC12A3

is a	snp
is	mentioned by
dbSNP	rs559626481
dbSNP (classic)	rs559626481
ClinGen	rs559626481
ebi	rs559626481
HLI	rs559626481
Exac	rs559626481
Gnomad	rs559626481
Varsome	rs559626481
LitVar	rs559626481
Map	rs559626481
PheGenI	rs559626481
Biobank	rs559626481
1000 genomes	rs559626481
hgdp	rs559626481
ensembl	rs559626481
geneview	rs559626481
scholar	rs559626481
google	rs559626481
pharmgkb	rs559626481
gwascentral	rs559626481
openSNP	rs559626481
23andMe	rs559626481
SNPshot	rs559626481
SNPdbe	rs559626481
MSV3d	rs559626481
GWAS Ctlg	rs559626481

Max Magnitude

0

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,