rs121909136

Orientation

plus

Stabilized

plus

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

Make rs121909136(A;A)

Make rs121909136(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

16055508

Gene

CLCNKB

is a	snp
is	mentioned by
dbSNP	rs121909136
dbSNP (classic)	rs121909136
ClinGen	rs121909136
ebi	rs121909136
HLI	rs121909136
Exac	rs121909136
Gnomad	rs121909136
Varsome	rs121909136
LitVar	rs121909136
Map	rs121909136
PheGenI	rs121909136
Biobank	rs121909136
1000 genomes	rs121909136
hgdp	rs121909136
ensembl	rs121909136
geneview	rs121909136
scholar	rs121909136
google	rs121909136
pharmgkb	rs121909136
gwascentral	rs121909136
openSNP	rs121909136
23andMe	rs121909136
SNPshot	rs121909136
SNPdbe	rs121909136
MSV3d	rs121909136
GWAS Ctlg	rs121909136

Max Magnitude

0

OMIM	602023
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121909136(A;A)
Alt	rs121909136(A;A)
Reference	Rs121909136(G;G)
Significance	Pathogenic
Disease	Bartter syndrome not provided
Variation	info
Gene	CLCNKB
CLNDBN	Bartter syndrome, type 3, with hypocalciuria not provided
Reversed	0
HGVS	NC_000001.10:g.16382003G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008037.3, RCV000413605.1,