rs1057517789

Orientation

plus

Stabilized

plus

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

Make rs1057517789(A;A)

Make rs1057517789(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22077539

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs1057517789
dbSNP (classic)	rs1057517789
ClinGen	rs1057517789
ebi	rs1057517789
HLI	rs1057517789
Exac	rs1057517789
Gnomad	rs1057517789
Varsome	rs1057517789
LitVar	rs1057517789
Map	rs1057517789
PheGenI	rs1057517789
Biobank	rs1057517789
1000 genomes	rs1057517789
hgdp	rs1057517789
ensembl	rs1057517789
geneview	rs1057517789
scholar	rs1057517789
google	rs1057517789
pharmgkb	rs1057517789
gwascentral	rs1057517789
openSNP	rs1057517789
23andMe	rs1057517789
SNPshot	rs1057517789
SNPdbe	rs1057517789
MSV3d	rs1057517789
GWAS Ctlg	rs1057517789

Max Magnitude

0

ClinVar
Risk	rs1057517789(A;A)
Alt	rs1057517789(A;A)
Reference	Rs1057517789(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22095657G>A
CLNSRC
CLNACC	RCV000413519.1,