rs1064795587

Orientation

plus

Stabilized

plus

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

Chromosome

17

Position

3659949

Gene	CTNS, LOC105371492

is a	snp
is	mentioned by
dbSNP	rs1064795587
dbSNP (classic)	rs1064795587
ClinGen	rs1064795587
ebi	rs1064795587
HLI	rs1064795587
Exac	rs1064795587
Gnomad	rs1064795587
Varsome	rs1064795587
LitVar	rs1064795587
Map	rs1064795587
PheGenI	rs1064795587
Biobank	rs1064795587
1000 genomes	rs1064795587
hgdp	rs1064795587
ensembl	rs1064795587
geneview	rs1064795587
scholar	rs1064795587
google	rs1064795587
pharmgkb	rs1064795587
gwascentral	rs1064795587
openSNP	rs1064795587
23andMe	rs1064795587
SNPshot	rs1064795587
SNPdbe	rs1064795587
MSV3d	rs1064795587
GWAS Ctlg	rs1064795587

Max Magnitude

0

ClinVar
Risk	rs1064795587(G;G)
Alt	rs1064795587(G;G)
Reference	Rs1064795587(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CTNS
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.3563243A>G
CLNSRC
CLNACC	RCV000479734.1,