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rs1057517904

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517904(C;C)
Make rs1057517904(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22133533
GenePHEX
is asnp
is mentioned by
dbSNPrs1057517904
dbSNP (old)rs1057517904
ClinGenrs1057517904
ebirs1057517904
HLIrs1057517904
Exacrs1057517904
Gnomadrs1057517904
Varsomers1057517904
Maprs1057517904
PheGenIrs1057517904
Biobankrs1057517904
1000 genomesrs1057517904
hgdprs1057517904
ensemblrs1057517904
gopubmedrs1057517904
geneviewrs1057517904
scholarrs1057517904
googlers1057517904
pharmgkbrs1057517904
gwascentralrs1057517904
openSNPrs1057517904
23andMers1057517904
23andMe allrs1057517904
SNPshotrs1057517904
SNPdbers1057517904
MSV3drs1057517904
GWAS Ctlgrs1057517904
Max Magnitude0
ClinVar
Risk rs1057517904(C;C)
Alt rs1057517904(C;C)
Reference Rs1057517904(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22151650T>C
CLNSRC
CLNACC RCV000413016.1,