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rs1064793227

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position22111561
GenePHEX
is asnp
is mentioned by
dbSNPrs1064793227
dbSNP (old)rs1064793227
ClinGenrs1064793227
ebirs1064793227
HLIrs1064793227
Exacrs1064793227
Gnomadrs1064793227
Varsomers1064793227
Maprs1064793227
PheGenIrs1064793227
Biobankrs1064793227
1000 genomesrs1064793227
hgdprs1064793227
ensemblrs1064793227
gopubmedrs1064793227
geneviewrs1064793227
scholarrs1064793227
googlers1064793227
pharmgkbrs1064793227
gwascentralrs1064793227
openSNPrs1064793227
23andMers1064793227
23andMe allrs1064793227
SNPshotrs1064793227
SNPdbers1064793227
MSV3drs1064793227
GWAS Ctlgrs1064793227
Max Magnitude0
ClinVar
Risk rs1064793227(C;C)
Alt rs1064793227(C;C)
Reference Rs1064793227(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22129679G>C
CLNSRC
CLNACC RCV000481043.1,