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rs1064793847

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position22114486
GenePHEX
is asnp
is mentioned by
dbSNPrs1064793847
dbSNP (old)rs1064793847
ClinGenrs1064793847
ebirs1064793847
HLIrs1064793847
Exacrs1064793847
Gnomadrs1064793847
Varsomers1064793847
Maprs1064793847
PheGenIrs1064793847
Biobankrs1064793847
1000 genomesrs1064793847
hgdprs1064793847
ensemblrs1064793847
gopubmedrs1064793847
geneviewrs1064793847
scholarrs1064793847
googlers1064793847
pharmgkbrs1064793847
gwascentralrs1064793847
openSNPrs1064793847
23andMers1064793847
23andMe allrs1064793847
SNPshotrs1064793847
SNPdbers1064793847
MSV3drs1064793847
GWAS Ctlgrs1064793847
Max Magnitude0
ClinVar
Risk rs1064793847(-;-)
Alt rs1064793847(-;-)
Reference Rs1064793847(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22132604delC
CLNSRC
CLNACC RCV000486397.1,