rs180177154

Orientation

plus

Stabilized

plus

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

Make rs180177154(A;A)

Make rs180177154(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

107649991

Gene

PRPS1

is a	snp
is	mentioned by
dbSNP	rs180177154
dbSNP (classic)	rs180177154
ClinGen	rs180177154
ebi	rs180177154
HLI	rs180177154
Exac	rs180177154
Gnomad	rs180177154
Varsome	rs180177154
LitVar	rs180177154
Map	rs180177154
PheGenI	rs180177154
Biobank	rs180177154
1000 genomes	rs180177154
hgdp	rs180177154
ensembl	rs180177154
geneview	rs180177154
scholar	rs180177154
google	rs180177154
pharmgkb	rs180177154
gwascentral	rs180177154
openSNP	rs180177154
23andMe	rs180177154
SNPshot	rs180177154
SNPdbe	rs180177154
MSV3d	rs180177154
GWAS Ctlg	rs180177154

Max Magnitude

0

ClinVar
Risk	rs180177154(A;A)
Alt	rs180177154(A;A)
Reference	Rs180177154(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	PRPS1
CLNDBN	Deafness, X-linked 1
Reversed	0
HGVS	NC_000023.10:g.106893221G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000010618.3,