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rs1064795106

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position22219049
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1064795106
dbSNP (classic)rs1064795106
ClinGenrs1064795106
ebirs1064795106
HLIrs1064795106
Exacrs1064795106
Gnomadrs1064795106
Varsomers1064795106
LitVarrs1064795106
Maprs1064795106
PheGenIrs1064795106
Biobankrs1064795106
1000 genomesrs1064795106
hgdprs1064795106
ensemblrs1064795106
geneviewrs1064795106
scholarrs1064795106
googlers1064795106
pharmgkbrs1064795106
gwascentralrs1064795106
openSNPrs1064795106
23andMers1064795106
23andMe allrs1064795106
SNPshotrs1064795106
SNPdbers1064795106
MSV3drs1064795106
GWAS Ctlgrs1064795106
Max Magnitude0
ClinVar
Risk rs1064795106(A;A)
Alt rs1064795106(A;A)
Reference Rs1064795106(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22237166G>A
CLNSRC
CLNACC RCV000481780.1,