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rs1064794305

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AATG;AATG) 0 common in clinvar
ChromosomeX
Position22219100
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1064794305
dbSNP (old)rs1064794305
ClinGenrs1064794305
ebirs1064794305
HLIrs1064794305
Exacrs1064794305
Gnomadrs1064794305
Varsomers1064794305
Maprs1064794305
PheGenIrs1064794305
Biobankrs1064794305
1000 genomesrs1064794305
hgdprs1064794305
ensemblrs1064794305
gopubmedrs1064794305
geneviewrs1064794305
scholarrs1064794305
googlers1064794305
pharmgkbrs1064794305
gwascentralrs1064794305
openSNPrs1064794305
23andMers1064794305
23andMe allrs1064794305
SNPshotrs1064794305
SNPdbers1064794305
MSV3drs1064794305
GWAS Ctlgrs1064794305
Max Magnitude0
ClinVar
Risk rs1064794305(-;-)
Alt rs1064794305(-;-)
Reference Rs1064794305(AATG;AATG)
Significance Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22237217_22237220delAATG
CLNSRC
CLNACC RCV000484521.1,