rs1057517790

Orientation

plus

Stabilized

plus

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

Make rs1057517790(C;T)

Make rs1057517790(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22077542

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs1057517790
dbSNP (classic)	rs1057517790
ClinGen	rs1057517790
ebi	rs1057517790
HLI	rs1057517790
Exac	rs1057517790
Gnomad	rs1057517790
Varsome	rs1057517790
LitVar	rs1057517790
Map	rs1057517790
PheGenI	rs1057517790
Biobank	rs1057517790
1000 genomes	rs1057517790
hgdp	rs1057517790
ensembl	rs1057517790
geneview	rs1057517790
scholar	rs1057517790
google	rs1057517790
pharmgkb	rs1057517790
gwascentral	rs1057517790
openSNP	rs1057517790
23andMe	rs1057517790
SNPshot	rs1057517790
SNPdbe	rs1057517790
MSV3d	rs1057517790
GWAS Ctlg	rs1057517790

Max Magnitude

0

ClinVar
Risk	rs1057517790(T;T)
Alt	rs1057517790(T;T)
Reference	Rs1057517790(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22095660C>T
CLNSRC
CLNACC	RCV000414149.1,