rs1057517792

Orientation

plus

Stabilized

plus

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

Make rs1057517792(-;A)

Make rs1057517792(A;A)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22099118

Gene

PHEX

is a	snp
is	mentioned by
dbSNP	rs1057517792
dbSNP (classic)	rs1057517792
ClinGen	rs1057517792
ebi	rs1057517792
HLI	rs1057517792
Exac	rs1057517792
Gnomad	rs1057517792
Varsome	rs1057517792
LitVar	rs1057517792
Map	rs1057517792
PheGenI	rs1057517792
Biobank	rs1057517792
1000 genomes	rs1057517792
hgdp	rs1057517792
ensembl	rs1057517792
geneview	rs1057517792
scholar	rs1057517792
google	rs1057517792
pharmgkb	rs1057517792
gwascentral	rs1057517792
openSNP	rs1057517792
23andMe	rs1057517792
SNPshot	rs1057517792
SNPdbe	rs1057517792
MSV3d	rs1057517792
GWAS Ctlg	rs1057517792

Max Magnitude

0

ClinVar
Risk	rs1057517792(A;A)
Alt	rs1057517792(A;A)
Reference	Rs1057517792(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22117236dupA
CLNSRC
CLNACC	RCV000414311.1,