rs1057518377

Orientation

plus

Stabilized

plus

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

Make rs1057518377(A;A)

Make rs1057518377(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22178378

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs1057518377
dbSNP (classic)	rs1057518377
ClinGen	rs1057518377
ebi	rs1057518377
HLI	rs1057518377
Exac	rs1057518377
Gnomad	rs1057518377
Varsome	rs1057518377
LitVar	rs1057518377
Map	rs1057518377
PheGenI	rs1057518377
Biobank	rs1057518377
1000 genomes	rs1057518377
hgdp	rs1057518377
ensembl	rs1057518377
geneview	rs1057518377
scholar	rs1057518377
google	rs1057518377
pharmgkb	rs1057518377
gwascentral	rs1057518377
openSNP	rs1057518377
23andMe	rs1057518377
SNPshot	rs1057518377
SNPdbe	rs1057518377
MSV3d	rs1057518377
GWAS Ctlg	rs1057518377

Max Magnitude

0

ClinVar
Risk	rs1057518377(A;A)
Alt	rs1057518377(A;A)
Reference	Rs1057518377(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22196495T>A
CLNSRC
CLNACC	RCV000414411.1,