rs1057517793

Orientation

plus

Stabilized

plus

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

Make rs1057517793(C;T)

Make rs1057517793(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22114464

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs1057517793
dbSNP (classic)	rs1057517793
ClinGen	rs1057517793
ebi	rs1057517793
HLI	rs1057517793
Exac	rs1057517793
Gnomad	rs1057517793
Varsome	rs1057517793
LitVar	rs1057517793
Map	rs1057517793
PheGenI	rs1057517793
Biobank	rs1057517793
1000 genomes	rs1057517793
hgdp	rs1057517793
ensembl	rs1057517793
geneview	rs1057517793
scholar	rs1057517793
google	rs1057517793
pharmgkb	rs1057517793
gwascentral	rs1057517793
openSNP	rs1057517793
23andMe	rs1057517793
SNPshot	rs1057517793
SNPdbe	rs1057517793
MSV3d	rs1057517793
GWAS Ctlg	rs1057517793

Max Magnitude

0

ClinVar
Risk	rs1057517793(T;T)
Alt	rs1057517793(T;T)
Reference	Rs1057517793(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22132582C>T
CLNSRC
CLNACC	RCV000413207.1,