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rs1064794849

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position22227602
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1064794849
dbSNP (old)rs1064794849
ClinGenrs1064794849
ebirs1064794849
HLIrs1064794849
Exacrs1064794849
Gnomadrs1064794849
Varsomers1064794849
Maprs1064794849
PheGenIrs1064794849
Biobankrs1064794849
1000 genomesrs1064794849
hgdprs1064794849
ensemblrs1064794849
gopubmedrs1064794849
geneviewrs1064794849
scholarrs1064794849
googlers1064794849
pharmgkbrs1064794849
gwascentralrs1064794849
openSNPrs1064794849
23andMers1064794849
23andMe allrs1064794849
SNPshotrs1064794849
SNPdbers1064794849
MSV3drs1064794849
GWAS Ctlgrs1064794849
Max Magnitude0
ClinVar
Risk rs1064794849(G;G)
Alt rs1064794849(G;G)
Reference Rs1064794849(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22245719T>G
CLNSRC
CLNACC RCV000486427.1,