rs180177151

Orientation

plus

Stabilized

plus

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

Make rs180177151(A;A)

Make rs180177151(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

107639365

Gene

PRPS1

is a	snp
is	mentioned by
dbSNP	rs180177151
dbSNP (classic)	rs180177151
ClinGen	rs180177151
ebi	rs180177151
HLI	rs180177151
Exac	rs180177151
Gnomad	rs180177151
Varsome	rs180177151
LitVar	rs180177151
Map	rs180177151
PheGenI	rs180177151
Biobank	rs180177151
1000 genomes	rs180177151
hgdp	rs180177151
ensembl	rs180177151
geneview	rs180177151
scholar	rs180177151
google	rs180177151
pharmgkb	rs180177151
gwascentral	rs180177151
openSNP	rs180177151
23andMe	rs180177151
SNPshot	rs180177151
SNPdbe	rs180177151
MSV3d	rs180177151
GWAS Ctlg	rs180177151

Max Magnitude

0

ClinVar
Risk	rs180177151(A;A)
Alt	rs180177151(A;A)
Reference	Rs180177151(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	PRPS1
CLNDBN	Deafness, X-linked 1
Reversed	0
HGVS	NC_000023.10:g.106882595G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000010616.3,