rs1057517904

Orientation

plus

Stabilized

plus

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

Make rs1057517904(C;C)

Make rs1057517904(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22133533

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs1057517904
dbSNP (classic)	rs1057517904
ClinGen	rs1057517904
ebi	rs1057517904
HLI	rs1057517904
Exac	rs1057517904
Gnomad	rs1057517904
Varsome	rs1057517904
LitVar	rs1057517904
Map	rs1057517904
PheGenI	rs1057517904
Biobank	rs1057517904
1000 genomes	rs1057517904
hgdp	rs1057517904
ensembl	rs1057517904
geneview	rs1057517904
scholar	rs1057517904
google	rs1057517904
pharmgkb	rs1057517904
gwascentral	rs1057517904
openSNP	rs1057517904
23andMe	rs1057517904
SNPshot	rs1057517904
SNPdbe	rs1057517904
MSV3d	rs1057517904
GWAS Ctlg	rs1057517904

Max Magnitude

0

ClinVar
Risk	rs1057517904(C;C)
Alt	rs1057517904(C;C)
Reference	Rs1057517904(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22151650T>C
CLNSRC
CLNACC	RCV000413016.1,