rs1057516207

Orientation

plus

Stabilized

plus

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

Make rs1057516207(-;A)

Make rs1057516207(A;A)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

16051793

Gene

CLCNKB

is a	snp
is	mentioned by
dbSNP	rs1057516207
dbSNP (classic)	rs1057516207
ClinGen	rs1057516207
ebi	rs1057516207
HLI	rs1057516207
Exac	rs1057516207
Gnomad	rs1057516207
Varsome	rs1057516207
LitVar	rs1057516207
Map	rs1057516207
PheGenI	rs1057516207
Biobank	rs1057516207
1000 genomes	rs1057516207
hgdp	rs1057516207
ensembl	rs1057516207
geneview	rs1057516207
scholar	rs1057516207
google	rs1057516207
pharmgkb	rs1057516207
gwascentral	rs1057516207
openSNP	rs1057516207
23andMe	rs1057516207
SNPshot	rs1057516207
SNPdbe	rs1057516207
MSV3d	rs1057516207
GWAS Ctlg	rs1057516207

Max Magnitude

0

ClinVar
Risk	rs1057516207(A;A)
Alt	rs1057516207(A;A)
Reference	Rs1057516207(-;-)
Significance	Pathogenic
Disease	Bartter syndrome type 3
Variation	info
Gene	CLCNKB
CLNDBN	Bartter syndrome type 3
Reversed	0
HGVS	NC_000001.10:g.16378288dupA
CLNSRC
CLNACC	RCV000408763.1,