rs879255615

Orientation

plus

Stabilized

plus

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

Make rs879255615(-;-)

Make rs879255615(-;A)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

3655095

Gene	CTNS, LOC105371492

is a	snp
is	mentioned by
dbSNP	rs879255615
dbSNP (classic)	rs879255615
ClinGen	rs879255615
ebi	rs879255615
HLI	rs879255615
Exac	rs879255615
Gnomad	rs879255615
Varsome	rs879255615
LitVar	rs879255615
Map	rs879255615
PheGenI	rs879255615
Biobank	rs879255615
1000 genomes	rs879255615
hgdp	rs879255615
ensembl	rs879255615
geneview	rs879255615
scholar	rs879255615
google	rs879255615
pharmgkb	rs879255615
gwascentral	rs879255615
openSNP	rs879255615
23andMe	rs879255615
SNPshot	rs879255615
SNPdbe	rs879255615
MSV3d	rs879255615
GWAS Ctlg	rs879255615

Max Magnitude

0

ClinVar
Risk	rs879255615(-;-)
Alt	rs879255615(-;-)
Reference	Rs879255615(A;A)
Significance	Pathogenic
Disease	Cystinosis
Variation	info
Gene	CTNS
CLNDBN	Cystinosis
Reversed	0
HGVS	NC_000017.10:g.3558389delA
CLNSRC
CLNACC	RCV000239704.1,