rs137853158

Orientation

plus

Stabilized

plus

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

Make rs137853158(G;T)

Make rs137853158(T;T)

Reference

GRCh38 38.1/141

Chromosome

15

Position

48229278

Gene	LOC105370807, SLC12A1

is a	snp
is	mentioned by
dbSNP	rs137853158
dbSNP (classic)	rs137853158
ClinGen	rs137853158
ebi	rs137853158
HLI	rs137853158
Exac	rs137853158
Gnomad	rs137853158
Varsome	rs137853158
LitVar	rs137853158
Map	rs137853158
PheGenI	rs137853158
Biobank	rs137853158
1000 genomes	rs137853158
hgdp	rs137853158
ensembl	rs137853158
geneview	rs137853158
scholar	rs137853158
google	rs137853158
pharmgkb	rs137853158
gwascentral	rs137853158
openSNP	rs137853158
23andMe	rs137853158
SNPshot	rs137853158
SNPdbe	rs137853158
MSV3d	rs137853158
GWAS Ctlg	rs137853158

Max Magnitude

0

OMIM	600839
Desc
Variant	0002
Related	also

ClinVar
Risk	rs137853158(T;T)
Alt	rs137853158(T;T)
Reference	Rs137853158(G;G)
Significance	Pathogenic
Disease	Bartter syndrome
Variation	info
Gene	SLC12A1
CLNDBN	Bartter syndrome, type 1, antenatal
Reversed	0
HGVS	NC_000015.9:g.48521475G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000009296.4,