rs180177153

Orientation

plus

Stabilized

plus

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

Make rs180177153(C;C)

Make rs180177153(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

107649944

Gene

PRPS1

is a	snp
is	mentioned by
dbSNP	rs180177153
dbSNP (classic)	rs180177153
ClinGen	rs180177153
ebi	rs180177153
HLI	rs180177153
Exac	rs180177153
Gnomad	rs180177153
Varsome	rs180177153
LitVar	rs180177153
Map	rs180177153
PheGenI	rs180177153
Biobank	rs180177153
1000 genomes	rs180177153
hgdp	rs180177153
ensembl	rs180177153
geneview	rs180177153
scholar	rs180177153
google	rs180177153
pharmgkb	rs180177153
gwascentral	rs180177153
openSNP	rs180177153
23andMe	rs180177153
SNPshot	rs180177153
SNPdbe	rs180177153
MSV3d	rs180177153
GWAS Ctlg	rs180177153

Max Magnitude

0

ClinVar
Risk	rs180177153(C;C)
Alt	rs180177153(C;C)
Reference	Rs180177153(T;T)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	PRPS1
CLNDBN	Deafness, X-linked 1
Reversed	0
HGVS	NC_000023.10:g.106893174T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000010619.3,