rs869025594

Orientation

plus

Stabilized

plus

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

Make rs869025594(C;C)

Make rs869025594(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

107628674

Gene

PRPS1

is a	snp
is	mentioned by
dbSNP	rs869025594
dbSNP (classic)	rs869025594
ClinGen	rs869025594
ebi	rs869025594
HLI	rs869025594
Exac	rs869025594
Gnomad	rs869025594
Varsome	rs869025594
LitVar	rs869025594
Map	rs869025594
PheGenI	rs869025594
Biobank	rs869025594
1000 genomes	rs869025594
hgdp	rs869025594
ensembl	rs869025594
geneview	rs869025594
scholar	rs869025594
google	rs869025594
pharmgkb	rs869025594
gwascentral	rs869025594
openSNP	rs869025594
23andMe	rs869025594
SNPshot	rs869025594
SNPdbe	rs869025594
MSV3d	rs869025594
GWAS Ctlg	rs869025594

Max Magnitude

0

ClinVar
Risk	rs869025594(C;C)
Alt	rs869025594(C;C)
Reference	Rs869025594(T;T)
Significance	Pathogenic
Disease	Charcot-Marie-Tooth disease
Variation	info
Gene	PRPS1
CLNDBN	Charcot-Marie-Tooth disease, X-linked recessive, type 5
Reversed	0
HGVS	NC_000023.10:g.106871904T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000208733.2,