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rs1064793229

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position22245400
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1064793229
dbSNP (old)rs1064793229
ClinGenrs1064793229
ebirs1064793229
HLIrs1064793229
Exacrs1064793229
Gnomadrs1064793229
Varsomers1064793229
Maprs1064793229
PheGenIrs1064793229
Biobankrs1064793229
1000 genomesrs1064793229
hgdprs1064793229
ensemblrs1064793229
gopubmedrs1064793229
geneviewrs1064793229
scholarrs1064793229
googlers1064793229
pharmgkbrs1064793229
gwascentralrs1064793229
openSNPrs1064793229
23andMers1064793229
23andMe allrs1064793229
SNPshotrs1064793229
SNPdbers1064793229
MSV3drs1064793229
GWAS Ctlgrs1064793229
Max Magnitude0
ClinVar
Risk rs1064793229(-;-)
Alt rs1064793229(-;-)
Reference Rs1064793229(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22263517delC
CLNSRC
CLNACC RCV000486516.1,