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rs1057521144

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521144(A;A)
Make rs1057521144(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22094100
GenePHEX
is asnp
is mentioned by
dbSNPrs1057521144
dbSNP (old)rs1057521144
ClinGenrs1057521144
ebirs1057521144
HLIrs1057521144
Exacrs1057521144
Gnomadrs1057521144
Varsomers1057521144
Maprs1057521144
PheGenIrs1057521144
Biobankrs1057521144
1000 genomesrs1057521144
hgdprs1057521144
ensemblrs1057521144
gopubmedrs1057521144
geneviewrs1057521144
scholarrs1057521144
googlers1057521144
pharmgkbrs1057521144
gwascentralrs1057521144
openSNPrs1057521144
23andMers1057521144
23andMe allrs1057521144
SNPshotrs1057521144
SNPdbers1057521144
MSV3drs1057521144
GWAS Ctlgrs1057521144
Max Magnitude0
ClinVar
Risk rs1057521144(A;A)
Alt rs1057521144(A;A)
Reference Rs1057521144(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22112218G>A
CLNSRC
CLNACC RCV000425906.1,