rs1057517795

Orientation

plus

Stabilized

plus

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

Make rs1057517795(A;A)

Make rs1057517795(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22219050

Gene	PHEX, PTCHD1-AS

is a	snp
is	mentioned by
dbSNP	rs1057517795
dbSNP (classic)	rs1057517795
ClinGen	rs1057517795
ebi	rs1057517795
HLI	rs1057517795
Exac	rs1057517795
Gnomad	rs1057517795
Varsome	rs1057517795
LitVar	rs1057517795
Map	rs1057517795
PheGenI	rs1057517795
Biobank	rs1057517795
1000 genomes	rs1057517795
hgdp	rs1057517795
ensembl	rs1057517795
geneview	rs1057517795
scholar	rs1057517795
google	rs1057517795
pharmgkb	rs1057517795
gwascentral	rs1057517795
openSNP	rs1057517795
23andMe	rs1057517795
SNPshot	rs1057517795
SNPdbe	rs1057517795
MSV3d	rs1057517795
GWAS Ctlg	rs1057517795

Max Magnitude

0

ClinVar
Risk	rs1057517795(A;A) rs1057517795(T;T)
Alt	rs1057517795(A;A) rs1057517795(T;T)
Reference	Rs1057517795(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PTCHD1-AS PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22237167G>A; NC_000023.10:g.22237167G>T
CLNSRC
CLNACC	RCV000413745.1, RCV000414654.1,