rs863224858

Orientation

plus

Stabilized

plus

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

Make rs863224858(-;-)

Make rs863224858(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

16055726

Gene

CLCNKB

is a	snp
is	mentioned by
dbSNP	rs863224858
dbSNP (classic)	rs863224858
ClinGen	rs863224858
ebi	rs863224858
HLI	rs863224858
Exac	rs863224858
Gnomad	rs863224858
Varsome	rs863224858
LitVar	rs863224858
Map	rs863224858
PheGenI	rs863224858
Biobank	rs863224858
1000 genomes	rs863224858
hgdp	rs863224858
ensembl	rs863224858
geneview	rs863224858
scholar	rs863224858
google	rs863224858
pharmgkb	rs863224858
gwascentral	rs863224858
openSNP	rs863224858
23andMe	rs863224858
SNPshot	rs863224858
SNPdbe	rs863224858
MSV3d	rs863224858
GWAS Ctlg	rs863224858

Max Magnitude

0

ClinVar
Risk	rs863224858(-;-)
Alt	rs863224858(-;-)
Reference	Rs863224858(C;C)
Significance	Probable-Pathogenic
Disease	Bartter syndrome type 3
Variation	info
Gene	CLCNKB
CLNDBN	Bartter syndrome type 3
Reversed	0
HGVS	NC_000001.10:g.16382221delC
CLNSRC
CLNACC	RCV000198263.1,