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rs1057517793

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517793(C;T)
Make rs1057517793(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22114464
GenePHEX
is asnp
is mentioned by
dbSNPrs1057517793
dbSNP (old)rs1057517793
ClinGenrs1057517793
ebirs1057517793
HLIrs1057517793
Exacrs1057517793
Gnomadrs1057517793
Varsomers1057517793
Maprs1057517793
PheGenIrs1057517793
Biobankrs1057517793
1000 genomesrs1057517793
hgdprs1057517793
ensemblrs1057517793
gopubmedrs1057517793
geneviewrs1057517793
scholarrs1057517793
googlers1057517793
pharmgkbrs1057517793
gwascentralrs1057517793
openSNPrs1057517793
23andMers1057517793
23andMe allrs1057517793
SNPshotrs1057517793
SNPdbers1057517793
MSV3drs1057517793
GWAS Ctlgrs1057517793
Max Magnitude0
ClinVar
Risk rs1057517793(T;T)
Alt rs1057517793(T;T)
Reference Rs1057517793(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22132582C>T
CLNSRC
CLNACC RCV000413207.1,