rs1057517800

Orientation

plus

Stabilized

plus

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

Make rs1057517800(-;-)

Make rs1057517800(-;CT)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22247947

Gene	PHEX, PTCHD1-AS

is a	snp
is	mentioned by
dbSNP	rs1057517800
dbSNP (classic)	rs1057517800
ClinGen	rs1057517800
ebi	rs1057517800
HLI	rs1057517800
Exac	rs1057517800
Gnomad	rs1057517800
Varsome	rs1057517800
LitVar	rs1057517800
Map	rs1057517800
PheGenI	rs1057517800
Biobank	rs1057517800
1000 genomes	rs1057517800
hgdp	rs1057517800
ensembl	rs1057517800
geneview	rs1057517800
scholar	rs1057517800
google	rs1057517800
pharmgkb	rs1057517800
gwascentral	rs1057517800
openSNP	rs1057517800
23andMe	rs1057517800
SNPshot	rs1057517800
SNPdbe	rs1057517800
MSV3d	rs1057517800
GWAS Ctlg	rs1057517800

Max Magnitude

0

ClinVar
Risk	rs1057517800(-;-)
Alt	rs1057517800(-;-)
Reference	Rs1057517800(CT;CT)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PTCHD1-AS PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22266064_22266065delCT
CLNSRC
CLNACC	RCV000413761.1,