rs1057516296

Orientation

plus

Stabilized

plus

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

Make rs1057516296(-;-)

Make rs1057516296(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

3655023

Gene	CTNS, LOC105371492

is a	snp
is	mentioned by
dbSNP	rs1057516296
dbSNP (classic)	rs1057516296
ClinGen	rs1057516296
ebi	rs1057516296
HLI	rs1057516296
Exac	rs1057516296
Gnomad	rs1057516296
Varsome	rs1057516296
LitVar	rs1057516296
Map	rs1057516296
PheGenI	rs1057516296
Biobank	rs1057516296
1000 genomes	rs1057516296
hgdp	rs1057516296
ensembl	rs1057516296
geneview	rs1057516296
scholar	rs1057516296
google	rs1057516296
pharmgkb	rs1057516296
gwascentral	rs1057516296
openSNP	rs1057516296
23andMe	rs1057516296
SNPshot	rs1057516296
SNPdbe	rs1057516296
MSV3d	rs1057516296
GWAS Ctlg	rs1057516296

Max Magnitude

0

ClinVar
Risk	rs1057516296(-;-)
Alt	rs1057516296(-;-)
Reference	Rs1057516296(A;A)
Significance	Probable-Pathogenic
Disease	Nephropathic cystinosis
Variation	info
Gene	CTNS
CLNDBN	Nephropathic cystinosis
Reversed	0
HGVS	NC_000017.10:g.3558317delA
CLNSRC
CLNACC	RCV000409604.1,