rs1057517788

Orientation

plus

Stabilized

plus

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

Make rs1057517788(C;C)

Make rs1057517788(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22076475

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs1057517788
dbSNP (classic)	rs1057517788
ClinGen	rs1057517788
ebi	rs1057517788
HLI	rs1057517788
Exac	rs1057517788
Gnomad	rs1057517788
Varsome	rs1057517788
LitVar	rs1057517788
Map	rs1057517788
PheGenI	rs1057517788
Biobank	rs1057517788
1000 genomes	rs1057517788
hgdp	rs1057517788
ensembl	rs1057517788
geneview	rs1057517788
scholar	rs1057517788
google	rs1057517788
pharmgkb	rs1057517788
gwascentral	rs1057517788
openSNP	rs1057517788
23andMe	rs1057517788
SNPshot	rs1057517788
SNPdbe	rs1057517788
MSV3d	rs1057517788
GWAS Ctlg	rs1057517788

Max Magnitude

0

ClinVar
Risk	rs1057517788(C;C)
Alt	rs1057517788(C;C)
Reference	Rs1057517788(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22094593G>C
CLNSRC
CLNACC	RCV000412890.1,