rs1057517980

Orientation

plus

Stabilized

plus

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

Make rs1057517980(G;T)

Make rs1057517980(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22219071

Gene	PHEX, PTCHD1-AS

is a	snp
is	mentioned by
dbSNP	rs1057517980
dbSNP (classic)	rs1057517980
ClinGen	rs1057517980
ebi	rs1057517980
HLI	rs1057517980
Exac	rs1057517980
Gnomad	rs1057517980
Varsome	rs1057517980
LitVar	rs1057517980
Map	rs1057517980
PheGenI	rs1057517980
Biobank	rs1057517980
1000 genomes	rs1057517980
hgdp	rs1057517980
ensembl	rs1057517980
geneview	rs1057517980
scholar	rs1057517980
google	rs1057517980
pharmgkb	rs1057517980
gwascentral	rs1057517980
openSNP	rs1057517980
23andMe	rs1057517980
SNPshot	rs1057517980
SNPdbe	rs1057517980
MSV3d	rs1057517980
GWAS Ctlg	rs1057517980

Max Magnitude

0

ClinVar
Risk	rs1057517980(A;A) rs1057517980(T;T)
Alt	rs1057517980(A;A) rs1057517980(T;T)
Reference	Rs1057517980(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PTCHD1-AS PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22237188G>A; NC_000023.10:g.22237188G>T
CLNSRC
CLNACC	RCV000419789.1, RCV000412906.1,