rs74315289

Orientation

plus

Stabilized

plus

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

Make rs74315289(A;A)

Make rs74315289(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

54999325

Gene

BSND

is a	snp
is	mentioned by
dbSNP	rs74315289
dbSNP (classic)	rs74315289
ClinGen	rs74315289
ebi	rs74315289
HLI	rs74315289
Exac	rs74315289
Gnomad	rs74315289
Varsome	rs74315289
LitVar	rs74315289
Map	rs74315289
PheGenI	rs74315289
Biobank	rs74315289
1000 genomes	rs74315289
hgdp	rs74315289
ensembl	rs74315289
geneview	rs74315289
scholar	rs74315289
google	rs74315289
pharmgkb	rs74315289
gwascentral	rs74315289
openSNP	rs74315289
23andMe	rs74315289
SNPshot	rs74315289
SNPdbe	rs74315289
MSV3d	rs74315289
GWAS Ctlg	rs74315289

Max Magnitude

0

OMIM	606412
Desc
Variant	0008
Related	also

ClinVar
Risk	rs74315289(A;A)
Alt	rs74315289(A;A)
Reference	Rs74315289(G;G)
Significance	Pathogenic
Disease	Bartter syndrome type 4
Variation	info
Gene	BSND
CLNDBN	Bartter syndrome type 4
Reversed	0
HGVS	NC_000001.10:g.55464998G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004637.4,