rs1057517796

Orientation

plus

Stabilized

plus

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

Make rs1057517796(-;T)

Make rs1057517796(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22219105

Gene	PHEX, PTCHD1-AS

is a	snp
is	mentioned by
dbSNP	rs1057517796
dbSNP (classic)	rs1057517796
ClinGen	rs1057517796
ebi	rs1057517796
HLI	rs1057517796
Exac	rs1057517796
Gnomad	rs1057517796
Varsome	rs1057517796
LitVar	rs1057517796
Map	rs1057517796
PheGenI	rs1057517796
Biobank	rs1057517796
1000 genomes	rs1057517796
hgdp	rs1057517796
ensembl	rs1057517796
geneview	rs1057517796
scholar	rs1057517796
google	rs1057517796
pharmgkb	rs1057517796
gwascentral	rs1057517796
openSNP	rs1057517796
23andMe	rs1057517796
SNPshot	rs1057517796
SNPdbe	rs1057517796
MSV3d	rs1057517796
GWAS Ctlg	rs1057517796

Max Magnitude

0

ClinVar
Risk	rs1057517796(T;T)
Alt	rs1057517796(T;T)
Reference	Rs1057517796(-;-)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PTCHD1-AS PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22237222dupT
CLNSRC
CLNACC	RCV000412973.1,