rs869025593

Orientation

plus

Stabilized

plus

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

Make rs869025593(A;C)

Make rs869025593(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

107647731

Gene

PRPS1

is a	snp
is	mentioned by
dbSNP	rs869025593
dbSNP (classic)	rs869025593
ClinGen	rs869025593
ebi	rs869025593
HLI	rs869025593
Exac	rs869025593
Gnomad	rs869025593
Varsome	rs869025593
LitVar	rs869025593
Map	rs869025593
PheGenI	rs869025593
Biobank	rs869025593
1000 genomes	rs869025593
hgdp	rs869025593
ensembl	rs869025593
geneview	rs869025593
scholar	rs869025593
google	rs869025593
pharmgkb	rs869025593
gwascentral	rs869025593
openSNP	rs869025593
23andMe	rs869025593
SNPshot	rs869025593
SNPdbe	rs869025593
MSV3d	rs869025593
GWAS Ctlg	rs869025593

Max Magnitude

0

ClinVar
Risk	rs869025593(C;C)
Alt	rs869025593(C;C)
Reference	Rs869025593(A;A)
Significance	Pathogenic
Disease	Deafness Arts syndrome
Variation	info
Gene	PRPS1
CLNDBN	Deafness, X-linked 1 Arts syndrome
Reversed	0
HGVS	NC_000023.10:g.106890961A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000208721.1, RCV000208743.1,