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rs1057517794

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517794(A;A)
Make rs1057517794(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22178272
GenePHEX
is asnp
is mentioned by
dbSNPrs1057517794
dbSNP (old)rs1057517794
ClinGenrs1057517794
ebirs1057517794
HLIrs1057517794
Exacrs1057517794
Gnomadrs1057517794
Varsomers1057517794
Maprs1057517794
PheGenIrs1057517794
Biobankrs1057517794
1000 genomesrs1057517794
hgdprs1057517794
ensemblrs1057517794
gopubmedrs1057517794
geneviewrs1057517794
scholarrs1057517794
googlers1057517794
pharmgkbrs1057517794
gwascentralrs1057517794
openSNPrs1057517794
23andMers1057517794
23andMe allrs1057517794
SNPshotrs1057517794
SNPdbers1057517794
MSV3drs1057517794
GWAS Ctlgrs1057517794
Max Magnitude0
ClinVar
Risk rs1057517794(A;A)
Alt rs1057517794(A;A)
Reference Rs1057517794(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22196389G>A
CLNSRC
CLNACC RCV000413596.1,