rs1057517791

Orientation

plus

Stabilized

plus

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

Make rs1057517791(-;-)

Make rs1057517791(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22096988

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs1057517791
dbSNP (classic)	rs1057517791
ClinGen	rs1057517791
ebi	rs1057517791
HLI	rs1057517791
Exac	rs1057517791
Gnomad	rs1057517791
Varsome	rs1057517791
LitVar	rs1057517791
Map	rs1057517791
PheGenI	rs1057517791
Biobank	rs1057517791
1000 genomes	rs1057517791
hgdp	rs1057517791
ensembl	rs1057517791
geneview	rs1057517791
scholar	rs1057517791
google	rs1057517791
pharmgkb	rs1057517791
gwascentral	rs1057517791
openSNP	rs1057517791
23andMe	rs1057517791
SNPshot	rs1057517791
SNPdbe	rs1057517791
MSV3d	rs1057517791
GWAS Ctlg	rs1057517791

Max Magnitude

0

ClinVar
Risk	rs1057517791(-;-)
Alt	rs1057517791(-;-)
Reference	Rs1057517791(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22115106delG
CLNSRC
CLNACC	RCV000413674.1,