rs587781261

Orientation

plus

Stabilized

plus

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

Make rs587781261(G;T)

Make rs587781261(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

107640932

Gene

PRPS1

is a	snp
is	mentioned by
dbSNP	rs587781261
dbSNP (classic)	rs587781261
ClinGen	rs587781261
ebi	rs587781261
HLI	rs587781261
Exac	rs587781261
Gnomad	rs587781261
Varsome	rs587781261
LitVar	rs587781261
Map	rs587781261
PheGenI	rs587781261
Biobank	rs587781261
1000 genomes	rs587781261
hgdp	rs587781261
ensembl	rs587781261
geneview	rs587781261
scholar	rs587781261
google	rs587781261
pharmgkb	rs587781261
gwascentral	rs587781261
openSNP	rs587781261
23andMe	rs587781261
SNPshot	rs587781261
SNPdbe	rs587781261
MSV3d	rs587781261
GWAS Ctlg	rs587781261

Max Magnitude

0

ClinVar
Risk	rs587781261(T;T)
Alt	rs587781261(T;T)
Reference	Rs587781261(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	PRPS1
CLNDBN	Deafness, X-linked 1
Reversed	0
HGVS	NC_000023.10:g.106884162G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000143857.3,