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

rs1057520756

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520756(C;C)
Make rs1057520756(C;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22219052
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1057520756
dbSNP (old)rs1057520756
ClinGenrs1057520756
ebirs1057520756
HLIrs1057520756
Exacrs1057520756
Gnomadrs1057520756
Varsomers1057520756
Maprs1057520756
PheGenIrs1057520756
Biobankrs1057520756
1000 genomesrs1057520756
hgdprs1057520756
ensemblrs1057520756
gopubmedrs1057520756
geneviewrs1057520756
scholarrs1057520756
googlers1057520756
pharmgkbrs1057520756
gwascentralrs1057520756
openSNPrs1057520756
23andMers1057520756
23andMe allrs1057520756
SNPshotrs1057520756
SNPdbers1057520756
MSV3drs1057520756
GWAS Ctlgrs1057520756
Max Magnitude0
ClinVar
Risk rs1057520756(C;C)
Alt rs1057520756(C;C)
Reference Rs1057520756(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22237169G>C
CLNSRC
CLNACC RCV000429437.1,