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rs1057517787

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517787(A;A)
Make rs1057517787(A;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22076464
GenePHEX
is asnp
is mentioned by
dbSNPrs1057517787
dbSNP (old)rs1057517787
ClinGenrs1057517787
ebirs1057517787
HLIrs1057517787
Exacrs1057517787
Gnomadrs1057517787
Varsomers1057517787
LitVarrs1057517787
Maprs1057517787
PheGenIrs1057517787
Biobankrs1057517787
1000 genomesrs1057517787
hgdprs1057517787
ensemblrs1057517787
gopubmedrs1057517787
geneviewrs1057517787
scholarrs1057517787
googlers1057517787
pharmgkbrs1057517787
gwascentralrs1057517787
openSNPrs1057517787
23andMers1057517787
23andMe allrs1057517787
SNPshotrs1057517787
SNPdbers1057517787
MSV3drs1057517787
GWAS Ctlgrs1057517787
Max Magnitude0
ClinVar
Risk rs1057517787(A;A)
Alt rs1057517787(A;A)
Reference Rs1057517787(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22094582C>A
CLNSRC
CLNACC RCV000414040.1,