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rs1057521143

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521143(C;T)
Make rs1057521143(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22077604
GenePHEX
is asnp
is mentioned by
dbSNPrs1057521143
dbSNP (old)rs1057521143
ClinGenrs1057521143
ebirs1057521143
HLIrs1057521143
Exacrs1057521143
Gnomadrs1057521143
Varsomers1057521143
LitVarrs1057521143
Maprs1057521143
PheGenIrs1057521143
Biobankrs1057521143
1000 genomesrs1057521143
hgdprs1057521143
ensemblrs1057521143
gopubmedrs1057521143
geneviewrs1057521143
scholarrs1057521143
googlers1057521143
pharmgkbrs1057521143
gwascentralrs1057521143
openSNPrs1057521143
23andMers1057521143
23andMe allrs1057521143
SNPshotrs1057521143
SNPdbers1057521143
MSV3drs1057521143
GWAS Ctlgrs1057521143
Max Magnitude0
ClinVar
Risk rs1057521143(T;T)
Alt rs1057521143(T;T)
Reference Rs1057521143(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22095722C>T
CLNSRC
CLNACC RCV000418710.1,