rs1057517896

Orientation

plus

Stabilized

plus

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

Make rs1057517896(C;C)

Make rs1057517896(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22111562

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs1057517896
dbSNP (classic)	rs1057517896
ClinGen	rs1057517896
ebi	rs1057517896
HLI	rs1057517896
Exac	rs1057517896
Gnomad	rs1057517896
Varsome	rs1057517896
LitVar	rs1057517896
Map	rs1057517896
PheGenI	rs1057517896
Biobank	rs1057517896
1000 genomes	rs1057517896
hgdp	rs1057517896
ensembl	rs1057517896
geneview	rs1057517896
scholar	rs1057517896
google	rs1057517896
pharmgkb	rs1057517896
gwascentral	rs1057517896
openSNP	rs1057517896
23andMe	rs1057517896
SNPshot	rs1057517896
SNPdbe	rs1057517896
MSV3d	rs1057517896
GWAS Ctlg	rs1057517896

Max Magnitude

0

ClinVar
Risk	rs1057517896(C;C)
Alt	rs1057517896(C;C)
Reference	Rs1057517896(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22129680T>C
CLNSRC
CLNACC	RCV000412709.1,