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rs1057517790

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517790(C;T)
Make rs1057517790(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22077542
GenePHEX
is asnp
is mentioned by
dbSNPrs1057517790
dbSNP (old)rs1057517790
ClinGenrs1057517790
ebirs1057517790
HLIrs1057517790
Exacrs1057517790
Gnomadrs1057517790
Varsomers1057517790
Maprs1057517790
PheGenIrs1057517790
Biobankrs1057517790
1000 genomesrs1057517790
hgdprs1057517790
ensemblrs1057517790
gopubmedrs1057517790
geneviewrs1057517790
scholarrs1057517790
googlers1057517790
pharmgkbrs1057517790
gwascentralrs1057517790
openSNPrs1057517790
23andMers1057517790
23andMe allrs1057517790
SNPshotrs1057517790
SNPdbers1057517790
MSV3drs1057517790
GWAS Ctlgrs1057517790
Max Magnitude0
ClinVar
Risk rs1057517790(T;T)
Alt rs1057517790(T;T)
Reference Rs1057517790(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22095660C>T
CLNSRC
CLNACC RCV000414149.1,