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rs1064794999

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position22245339
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1064794999
dbSNP (old)rs1064794999
ClinGenrs1064794999
ebirs1064794999
HLIrs1064794999
Exacrs1064794999
Gnomadrs1064794999
Varsomers1064794999
Maprs1064794999
PheGenIrs1064794999
Biobankrs1064794999
1000 genomesrs1064794999
hgdprs1064794999
ensemblrs1064794999
gopubmedrs1064794999
geneviewrs1064794999
scholarrs1064794999
googlers1064794999
pharmgkbrs1064794999
gwascentralrs1064794999
openSNPrs1064794999
23andMers1064794999
23andMe allrs1064794999
SNPshotrs1064794999
SNPdbers1064794999
MSV3drs1064794999
GWAS Ctlgrs1064794999
Max Magnitude0
ClinVar
Risk rs1064794999(C;C)
Alt rs1064794999(C;C)
Reference Rs1064794999(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22263456T>C
CLNSRC
CLNACC RCV000478010.1,