rs1057517979

Orientation

plus

Stabilized

plus

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

Make rs1057517979(-;-)

Make rs1057517979(-;TAATTGTCGGAC)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

22219062

Gene	PHEX, PTCHD1-AS

is a	snp
is	mentioned by
dbSNP	rs1057517979
dbSNP (classic)	rs1057517979
ClinGen	rs1057517979
ebi	rs1057517979
HLI	rs1057517979
Exac	rs1057517979
Gnomad	rs1057517979
Varsome	rs1057517979
LitVar	rs1057517979
Map	rs1057517979
PheGenI	rs1057517979
Biobank	rs1057517979
1000 genomes	rs1057517979
hgdp	rs1057517979
ensembl	rs1057517979
geneview	rs1057517979
scholar	rs1057517979
google	rs1057517979
pharmgkb	rs1057517979
gwascentral	rs1057517979
openSNP	rs1057517979
23andMe	rs1057517979
SNPshot	rs1057517979
SNPdbe	rs1057517979
MSV3d	rs1057517979
GWAS Ctlg	rs1057517979

Max Magnitude

0

ClinVar
Risk	rs1057517979(-;-)
Alt	rs1057517979(-;-)
Reference	Rs1057517979(TAATTGTCGGAC;TAATTGTCGGAC)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PTCHD1-AS PHEX
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.22237179_22237190delTAATTGTCGGAC
CLNSRC
CLNACC	RCV000414105.1,