rs1057517794

Orientation

plus

Stabilized

plus

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

Make rs1057517794(A;A)

Make rs1057517794(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22178272

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs1057517794
dbSNP (classic)	rs1057517794
ClinGen	rs1057517794
ebi	rs1057517794
HLI	rs1057517794
Exac	rs1057517794
Gnomad	rs1057517794
Varsome	rs1057517794
LitVar	rs1057517794
Map	rs1057517794
PheGenI	rs1057517794
Biobank	rs1057517794
1000 genomes	rs1057517794
hgdp	rs1057517794
ensembl	rs1057517794
geneview	rs1057517794
scholar	rs1057517794
google	rs1057517794
pharmgkb	rs1057517794
gwascentral	rs1057517794
openSNP	rs1057517794
23andMe	rs1057517794
SNPshot	rs1057517794
SNPdbe	rs1057517794
MSV3d	rs1057517794
GWAS Ctlg	rs1057517794

Max Magnitude

0

ClinVar
Risk	rs1057517794(A;A)
Alt	rs1057517794(A;A)
Reference	Rs1057517794(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22196389G>A
CLNSRC
CLNACC	RCV000413596.1,