rs1057517787

Orientation

plus

Stabilized

plus

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

Make rs1057517787(A;A)

Make rs1057517787(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22076464

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs1057517787
dbSNP (classic)	rs1057517787
ClinGen	rs1057517787
ebi	rs1057517787
HLI	rs1057517787
Exac	rs1057517787
Gnomad	rs1057517787
Varsome	rs1057517787
LitVar	rs1057517787
Map	rs1057517787
PheGenI	rs1057517787
Biobank	rs1057517787
1000 genomes	rs1057517787
hgdp	rs1057517787
ensembl	rs1057517787
geneview	rs1057517787
scholar	rs1057517787
google	rs1057517787
pharmgkb	rs1057517787
gwascentral	rs1057517787
openSNP	rs1057517787
23andMe	rs1057517787
SNPshot	rs1057517787
SNPdbe	rs1057517787
MSV3d	rs1057517787
GWAS Ctlg	rs1057517787

Max Magnitude

0

ClinVar
Risk	rs1057517787(A;A)
Alt	rs1057517787(A;A)
Reference	Rs1057517787(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22094582C>A
CLNSRC
CLNACC	RCV000414040.1,