rs121908125

Orientation

plus

Stabilized

plus

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

Make rs121908125(A;A)

Make rs121908125(A;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

3655304

Gene	CTNS, LOC105371492

is a	snp
is	mentioned by
dbSNP	rs121908125
dbSNP (classic)	rs121908125
ClinGen	rs121908125
ebi	rs121908125
HLI	rs121908125
Exac	rs121908125
Gnomad	rs121908125
Varsome	rs121908125
LitVar	rs121908125
Map	rs121908125
PheGenI	rs121908125
Biobank	rs121908125
1000 genomes	rs121908125
hgdp	rs121908125
ensembl	rs121908125
geneview	rs121908125
scholar	rs121908125
google	rs121908125
pharmgkb	rs121908125
gwascentral	rs121908125
openSNP	rs121908125
23andMe	rs121908125
SNPshot	rs121908125
SNPdbe	rs121908125
MSV3d	rs121908125
GWAS Ctlg	rs121908125

Max Magnitude

0

OMIM	606272
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121908125(A;A)
Alt	rs121908125(A;A)
Reference	Rs121908125(G;G)
Significance	Untested
Disease	Cystinosis
Variation	info
Gene	CTNS
CLNDBN	Cystinosis
Reversed	0
HGVS	NC_000017.10:g.3558598G>A
CLNSRC	OMIM Allelic Variant GeneReviews
CLNACC	SCV000024868.1, SCV000024868.1, SCV000041133.1, SCV000041133.1,