rs121909138

Orientation

plus

Stabilized

plus

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

Make rs121909138(C;T)

Make rs121909138(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

16027432

Gene

CLCNKA

is a	snp
is	mentioned by
dbSNP	rs121909138
dbSNP (classic)	rs121909138
ClinGen	rs121909138
ebi	rs121909138
HLI	rs121909138
Exac	rs121909138
Gnomad	rs121909138
Varsome	rs121909138
LitVar	rs121909138
Map	rs121909138
PheGenI	rs121909138
Biobank	rs121909138
1000 genomes	rs121909138
hgdp	rs121909138
ensembl	rs121909138
geneview	rs121909138
scholar	rs121909138
google	rs121909138
pharmgkb	rs121909138
gwascentral	rs121909138
openSNP	rs121909138
23andMe	rs121909138
SNPshot	rs121909138
SNPdbe	rs121909138
MSV3d	rs121909138
GWAS Ctlg	rs121909138

Max Magnitude

0

OMIM	602024
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121909138(T;T)
Alt	rs121909138(T;T)
Reference	Rs121909138(C;C)
Significance	Pathogenic
Disease	Bartter syndrome
Variation	info
Gene	CLCNKA
CLNDBN	Bartter syndrome, type 4b
Reversed	0
HGVS	NC_000001.10:g.16353927C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008028.2,