rs1064796391

Orientation

plus

Stabilized

plus

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

Chromosome

X

Position

22094011

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs1064796391
dbSNP (classic)	rs1064796391
ClinGen	rs1064796391
ebi	rs1064796391
HLI	rs1064796391
Exac	rs1064796391
Gnomad	rs1064796391
Varsome	rs1064796391
LitVar	rs1064796391
Map	rs1064796391
PheGenI	rs1064796391
Biobank	rs1064796391
1000 genomes	rs1064796391
hgdp	rs1064796391
ensembl	rs1064796391
geneview	rs1064796391
scholar	rs1064796391
google	rs1064796391
pharmgkb	rs1064796391
gwascentral	rs1064796391
openSNP	rs1064796391
23andMe	rs1064796391
SNPshot	rs1064796391
SNPdbe	rs1064796391
MSV3d	rs1064796391
GWAS Ctlg	rs1064796391

Max Magnitude

0

ClinVar
Risk	rs1064796391(-;-)
Alt	rs1064796391(-;-)
Reference	Rs1064796391(TGG;TGG)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22112129_22112131delTGG
CLNSRC
CLNACC	RCV000480929.1,