rs879255613

Orientation

plus

Stabilized

plus

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

Make rs879255613(-;G)

Make rs879255613(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

3647473

Gene	CTNS, LOC105371493

is a	snp
is	mentioned by
dbSNP	rs879255613
dbSNP (classic)	rs879255613
ClinGen	rs879255613
ebi	rs879255613
HLI	rs879255613
Exac	rs879255613
Gnomad	rs879255613
Varsome	rs879255613
LitVar	rs879255613
Map	rs879255613
PheGenI	rs879255613
Biobank	rs879255613
1000 genomes	rs879255613
hgdp	rs879255613
ensembl	rs879255613
geneview	rs879255613
scholar	rs879255613
google	rs879255613
pharmgkb	rs879255613
gwascentral	rs879255613
openSNP	rs879255613
23andMe	rs879255613
SNPshot	rs879255613
SNPdbe	rs879255613
MSV3d	rs879255613
GWAS Ctlg	rs879255613

Max Magnitude

0

ClinVar
Risk	rs879255613(G;G)
Alt	rs879255613(G;G)
Reference	Rs879255613(-;-)
Significance	Pathogenic
Disease	Cystinosis
Variation	info
Gene	CTNS
CLNDBN	Cystinosis
Reversed	0
HGVS	NC_000017.10:g.3550767dupG
CLNSRC
CLNACC	RCV000239715.1,