rs1057517797

Orientation

plus

Stabilized

plus

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

Make rs1057517797(C;C)

Make rs1057517797(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22227616

Gene	PHEX, PTCHD1-AS

is a	snp
is	mentioned by
dbSNP	rs1057517797
dbSNP (classic)	rs1057517797
ClinGen	rs1057517797
ebi	rs1057517797
HLI	rs1057517797
Exac	rs1057517797
Gnomad	rs1057517797
Varsome	rs1057517797
LitVar	rs1057517797
Map	rs1057517797
PheGenI	rs1057517797
Biobank	rs1057517797
1000 genomes	rs1057517797
hgdp	rs1057517797
ensembl	rs1057517797
geneview	rs1057517797
scholar	rs1057517797
google	rs1057517797
pharmgkb	rs1057517797
gwascentral	rs1057517797
openSNP	rs1057517797
23andMe	rs1057517797
SNPshot	rs1057517797
SNPdbe	rs1057517797
MSV3d	rs1057517797
GWAS Ctlg	rs1057517797

Max Magnitude

0

ClinVar
Risk	rs1057517797(C;C)
Alt	rs1057517797(C;C)
Reference	Rs1057517797(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PTCHD1-AS PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22245733G>C
CLNSRC
CLNACC	RCV000413865.1,