rs1057517798

Orientation

plus

Stabilized

plus

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

Make rs1057517798(A;A)

Make rs1057517798(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22247862

Gene	PHEX, PTCHD1-AS

is a	snp
is	mentioned by
dbSNP	rs1057517798
dbSNP (classic)	rs1057517798
ClinGen	rs1057517798
ebi	rs1057517798
HLI	rs1057517798
Exac	rs1057517798
Gnomad	rs1057517798
Varsome	rs1057517798
LitVar	rs1057517798
Map	rs1057517798
PheGenI	rs1057517798
Biobank	rs1057517798
1000 genomes	rs1057517798
hgdp	rs1057517798
ensembl	rs1057517798
geneview	rs1057517798
scholar	rs1057517798
google	rs1057517798
pharmgkb	rs1057517798
gwascentral	rs1057517798
openSNP	rs1057517798
23andMe	rs1057517798
SNPshot	rs1057517798
SNPdbe	rs1057517798
MSV3d	rs1057517798
GWAS Ctlg	rs1057517798

Max Magnitude

0

ClinVar
Risk	rs1057517798(A;A)
Alt	rs1057517798(A;A)
Reference	Rs1057517798(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PTCHD1-AS PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22265979C>A
CLNSRC
CLNACC	RCV000414545.1,