rs202114767

Orientation

plus

Stabilized

plus

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

Make rs202114767(A;A)

Make rs202114767(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

56904402

Gene	MIR6863, SLC12A3

is a	snp
is	mentioned by
dbSNP	rs202114767
dbSNP (classic)	rs202114767
ClinGen	rs202114767
ebi	rs202114767
HLI	rs202114767
Exac	rs202114767
Gnomad	rs202114767
Varsome	rs202114767
LitVar	rs202114767
Map	rs202114767
PheGenI	rs202114767
Biobank	rs202114767
1000 genomes	rs202114767
hgdp	rs202114767
ensembl	rs202114767
geneview	rs202114767
scholar	rs202114767
google	rs202114767
pharmgkb	rs202114767
gwascentral	rs202114767
openSNP	rs202114767
23andMe	rs202114767
SNPshot	rs202114767
SNPdbe	rs202114767
MSV3d	rs202114767
GWAS Ctlg	rs202114767

Max Magnitude

0

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,