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rs1057517788

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517788(C;C)
Make rs1057517788(C;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22076475
GenePHEX
is asnp
is mentioned by
dbSNPrs1057517788
dbSNP (old)rs1057517788
ClinGenrs1057517788
ebirs1057517788
HLIrs1057517788
Exacrs1057517788
Gnomadrs1057517788
Varsomers1057517788
Maprs1057517788
PheGenIrs1057517788
Biobankrs1057517788
1000 genomesrs1057517788
hgdprs1057517788
ensemblrs1057517788
gopubmedrs1057517788
geneviewrs1057517788
scholarrs1057517788
googlers1057517788
pharmgkbrs1057517788
gwascentralrs1057517788
openSNPrs1057517788
23andMers1057517788
23andMe allrs1057517788
SNPshotrs1057517788
SNPdbers1057517788
MSV3drs1057517788
GWAS Ctlgrs1057517788
Max Magnitude0
ClinVar
Risk rs1057517788(C;C)
Alt rs1057517788(C;C)
Reference Rs1057517788(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22094593G>C
CLNSRC
CLNACC RCV000412890.1,