rs1057518348

Orientation

plus

Stabilized

plus

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

Make rs1057518348(A;A)

Make rs1057518348(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22077704

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs1057518348
dbSNP (classic)	rs1057518348
ClinGen	rs1057518348
ebi	rs1057518348
HLI	rs1057518348
Exac	rs1057518348
Gnomad	rs1057518348
Varsome	rs1057518348
LitVar	rs1057518348
Map	rs1057518348
PheGenI	rs1057518348
Biobank	rs1057518348
1000 genomes	rs1057518348
hgdp	rs1057518348
ensembl	rs1057518348
geneview	rs1057518348
scholar	rs1057518348
google	rs1057518348
pharmgkb	rs1057518348
gwascentral	rs1057518348
openSNP	rs1057518348
23andMe	rs1057518348
SNPshot	rs1057518348
SNPdbe	rs1057518348
MSV3d	rs1057518348
GWAS Ctlg	rs1057518348

Max Magnitude

0

ClinVar
Risk	rs1057518348(A;A)
Alt	rs1057518348(A;A)
Reference	Rs1057518348(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22095822T>A
CLNSRC
CLNACC	RCV000413368.1,