rs1057521143

Orientation

plus

Stabilized

plus

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

Make rs1057521143(C;T)

Make rs1057521143(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22077604

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs1057521143
dbSNP (classic)	rs1057521143
ClinGen	rs1057521143
ebi	rs1057521143
HLI	rs1057521143
Exac	rs1057521143
Gnomad	rs1057521143
Varsome	rs1057521143
LitVar	rs1057521143
Map	rs1057521143
PheGenI	rs1057521143
Biobank	rs1057521143
1000 genomes	rs1057521143
hgdp	rs1057521143
ensembl	rs1057521143
geneview	rs1057521143
scholar	rs1057521143
google	rs1057521143
pharmgkb	rs1057521143
gwascentral	rs1057521143
openSNP	rs1057521143
23andMe	rs1057521143
SNPshot	rs1057521143
SNPdbe	rs1057521143
MSV3d	rs1057521143
GWAS Ctlg	rs1057521143

Max Magnitude

0

ClinVar
Risk	rs1057521143(T;T)
Alt	rs1057521143(T;T)
Reference	Rs1057521143(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22095722C>T
CLNSRC
CLNACC	RCV000418710.1,