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rs1064794150

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position22247900
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1064794150
dbSNP (old)rs1064794150
ClinGenrs1064794150
ebirs1064794150
HLIrs1064794150
Exacrs1064794150
Gnomadrs1064794150
Varsomers1064794150
Maprs1064794150
PheGenIrs1064794150
Biobankrs1064794150
1000 genomesrs1064794150
hgdprs1064794150
ensemblrs1064794150
gopubmedrs1064794150
geneviewrs1064794150
scholarrs1064794150
googlers1064794150
pharmgkbrs1064794150
gwascentralrs1064794150
openSNPrs1064794150
23andMers1064794150
23andMe allrs1064794150
SNPshotrs1064794150
SNPdbers1064794150
MSV3drs1064794150
GWAS Ctlgrs1064794150
Max Magnitude0
ClinVar
Risk rs1064794150(C;C)
Alt rs1064794150(C;C)
Reference Rs1064794150(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22266017T>C
CLNSRC
CLNACC RCV000479634.1,