rs1057518596

Orientation

plus

Stabilized

plus

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

Make rs1057518596(A;A)

Make rs1057518596(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22227612

Gene	PHEX, PTCHD1-AS

is a	snp
is	mentioned by
dbSNP	rs1057518596
dbSNP (classic)	rs1057518596
ClinGen	rs1057518596
ebi	rs1057518596
HLI	rs1057518596
Exac	rs1057518596
Gnomad	rs1057518596
Varsome	rs1057518596
LitVar	rs1057518596
Map	rs1057518596
PheGenI	rs1057518596
Biobank	rs1057518596
1000 genomes	rs1057518596
hgdp	rs1057518596
ensembl	rs1057518596
geneview	rs1057518596
scholar	rs1057518596
google	rs1057518596
pharmgkb	rs1057518596
gwascentral	rs1057518596
openSNP	rs1057518596
23andMe	rs1057518596
SNPshot	rs1057518596
SNPdbe	rs1057518596
MSV3d	rs1057518596
GWAS Ctlg	rs1057518596

Max Magnitude

0

ClinVar
Risk	rs1057518596(A;A)
Alt	rs1057518596(A;A)
Reference	Rs1057518596(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PTCHD1-AS PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22245729G>A
CLNSRC
CLNACC	RCV000413408.1,