Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057517798

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517798(A;A)
Make rs1057517798(A;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22247862
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1057517798
dbSNP (old)rs1057517798
ClinGenrs1057517798
ebirs1057517798
HLIrs1057517798
Exacrs1057517798
Gnomadrs1057517798
Varsomers1057517798
Maprs1057517798
PheGenIrs1057517798
Biobankrs1057517798
1000 genomesrs1057517798
hgdprs1057517798
ensemblrs1057517798
gopubmedrs1057517798
geneviewrs1057517798
scholarrs1057517798
googlers1057517798
pharmgkbrs1057517798
gwascentralrs1057517798
openSNPrs1057517798
23andMers1057517798
23andMe allrs1057517798
SNPshotrs1057517798
SNPdbers1057517798
MSV3drs1057517798
GWAS Ctlgrs1057517798
Max Magnitude0
ClinVar
Risk rs1057517798(A;A)
Alt rs1057517798(A;A)
Reference Rs1057517798(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22265979C>A
CLNSRC
CLNACC RCV000414545.1,