rs193922460

Orientation

plus

Stabilized

plus

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

Make rs193922460(-;CC)

Make rs193922460(CC;CC)

Reference

GRCh38 38.1/141

Chromosome

X

Position

22096990

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs193922460
dbSNP (classic)	rs193922460
ClinGen	rs193922460
ebi	rs193922460
HLI	rs193922460
Exac	rs193922460
Gnomad	rs193922460
Varsome	rs193922460
LitVar	rs193922460
Map	rs193922460
PheGenI	rs193922460
Biobank	rs193922460
1000 genomes	rs193922460
hgdp	rs193922460
ensembl	rs193922460
geneview	rs193922460
scholar	rs193922460
google	rs193922460
pharmgkb	rs193922460
gwascentral	rs193922460
openSNP	rs193922460
23andMe	rs193922460
SNPshot	rs193922460
SNPdbe	rs193922460
MSV3d	rs193922460
GWAS Ctlg	rs193922460

Max Magnitude

0

ClinVar
Risk	rs193922460(CC;CC)
Alt	rs193922460(CC;CC)
Reference	Rs193922460(-;-)
Significance	Probable-Pathogenic
Disease	Familial X-linked hypophosphatemic vitamin D refractory rickets
Variation	info
Gene	PHEX
CLNDBN	Familial X-linked hypophosphatemic vitamin D refractory rickets
Reversed	0
HGVS	NC_000023.10:g.22115107_22115108dupCC
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030358.1,