rs1057517981

Orientation

plus

Stabilized

plus

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

Make rs1057517981(A;A)

Make rs1057517981(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22247901

Gene	PHEX, PTCHD1-AS

is a	snp
is	mentioned by
dbSNP	rs1057517981
dbSNP (classic)	rs1057517981
ClinGen	rs1057517981
ebi	rs1057517981
HLI	rs1057517981
Exac	rs1057517981
Gnomad	rs1057517981
Varsome	rs1057517981
LitVar	rs1057517981
Map	rs1057517981
PheGenI	rs1057517981
Biobank	rs1057517981
1000 genomes	rs1057517981
hgdp	rs1057517981
ensembl	rs1057517981
geneview	rs1057517981
scholar	rs1057517981
google	rs1057517981
pharmgkb	rs1057517981
gwascentral	rs1057517981
openSNP	rs1057517981
23andMe	rs1057517981
SNPshot	rs1057517981
SNPdbe	rs1057517981
MSV3d	rs1057517981
GWAS Ctlg	rs1057517981

Max Magnitude

0

ClinVar
Risk	rs1057517981(A;A)
Alt	rs1057517981(A;A)
Reference	Rs1057517981(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PTCHD1-AS PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22266018G>A
CLNSRC
CLNACC	RCV000413547.1,