rs1057520756

Orientation

plus

Stabilized

plus

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

Make rs1057520756(C;C)

Make rs1057520756(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22219052

Gene	PHEX, PTCHD1-AS

is a	snp
is	mentioned by
dbSNP	rs1057520756
dbSNP (classic)	rs1057520756
ClinGen	rs1057520756
ebi	rs1057520756
HLI	rs1057520756
Exac	rs1057520756
Gnomad	rs1057520756
Varsome	rs1057520756
LitVar	rs1057520756
Map	rs1057520756
PheGenI	rs1057520756
Biobank	rs1057520756
1000 genomes	rs1057520756
hgdp	rs1057520756
ensembl	rs1057520756
geneview	rs1057520756
scholar	rs1057520756
google	rs1057520756
pharmgkb	rs1057520756
gwascentral	rs1057520756
openSNP	rs1057520756
23andMe	rs1057520756
SNPshot	rs1057520756
SNPdbe	rs1057520756
MSV3d	rs1057520756
GWAS Ctlg	rs1057520756

Max Magnitude

0

ClinVar
Risk	rs1057520756(C;C)
Alt	rs1057520756(C;C)
Reference	Rs1057520756(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PTCHD1-AS PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22237169G>C
CLNSRC
CLNACC	RCV000429437.1,