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rs1057520582

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520582(G;T)
Make rs1057520582(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22212959
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1057520582
dbSNP (old)rs1057520582
ClinGenrs1057520582
ebirs1057520582
HLIrs1057520582
Exacrs1057520582
Gnomadrs1057520582
Varsomers1057520582
Maprs1057520582
PheGenIrs1057520582
Biobankrs1057520582
1000 genomesrs1057520582
hgdprs1057520582
ensemblrs1057520582
gopubmedrs1057520582
geneviewrs1057520582
scholarrs1057520582
googlers1057520582
pharmgkbrs1057520582
gwascentralrs1057520582
openSNPrs1057520582
23andMers1057520582
23andMe allrs1057520582
SNPshotrs1057520582
SNPdbers1057520582
MSV3drs1057520582
GWAS Ctlgrs1057520582
Max Magnitude0
ClinVar
Risk rs1057520582(T;T)
Alt rs1057520582(T;T)
Reference Rs1057520582(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22231076G>T
CLNSRC
CLNACC RCV000424738.1,