rs74315288

Orientation

plus

Stabilized

plus

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

Make rs74315288(G;T)

Make rs74315288(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

54999209

Gene

BSND

is a	snp
is	mentioned by
dbSNP	rs74315288
dbSNP (classic)	rs74315288
ClinGen	rs74315288
ebi	rs74315288
HLI	rs74315288
Exac	rs74315288
Gnomad	rs74315288
Varsome	rs74315288
LitVar	rs74315288
Map	rs74315288
PheGenI	rs74315288
Biobank	rs74315288
1000 genomes	rs74315288
hgdp	rs74315288
ensembl	rs74315288
geneview	rs74315288
scholar	rs74315288
google	rs74315288
pharmgkb	rs74315288
gwascentral	rs74315288
openSNP	rs74315288
23andMe	rs74315288
SNPshot	rs74315288
SNPdbe	rs74315288
MSV3d	rs74315288
GWAS Ctlg	rs74315288

Max Magnitude

0

OMIM	606412
Desc
Variant	0007
Related	also

ClinVar
Risk	rs74315288(A;A) rs74315288(T;T)
Alt	rs74315288(A;A) rs74315288(T;T)
Reference	Rs74315288(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.55464882G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004636.3,