rs1057518214

Orientation

plus

Stabilized

plus

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

Make rs1057518214(G;G)

Make rs1057518214(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22178382

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs1057518214
dbSNP (classic)	rs1057518214
ClinGen	rs1057518214
ebi	rs1057518214
HLI	rs1057518214
Exac	rs1057518214
Gnomad	rs1057518214
Varsome	rs1057518214
LitVar	rs1057518214
Map	rs1057518214
PheGenI	rs1057518214
Biobank	rs1057518214
1000 genomes	rs1057518214
hgdp	rs1057518214
ensembl	rs1057518214
geneview	rs1057518214
scholar	rs1057518214
google	rs1057518214
pharmgkb	rs1057518214
gwascentral	rs1057518214
openSNP	rs1057518214
23andMe	rs1057518214
SNPshot	rs1057518214
SNPdbe	rs1057518214
MSV3d	rs1057518214
GWAS Ctlg	rs1057518214

Max Magnitude

0

ClinVar
Risk	rs1057518214(G;G)
Alt	rs1057518214(G;G)
Reference	Rs1057518214(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22196499T>G
CLNSRC
CLNACC	RCV000412767.1,