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rs1064796845

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position22245341
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1064796845
dbSNP (old)rs1064796845
ClinGenrs1064796845
ebirs1064796845
HLIrs1064796845
Exacrs1064796845
Gnomadrs1064796845
Varsomers1064796845
Maprs1064796845
PheGenIrs1064796845
Biobankrs1064796845
1000 genomesrs1064796845
hgdprs1064796845
ensemblrs1064796845
gopubmedrs1064796845
geneviewrs1064796845
scholarrs1064796845
googlers1064796845
pharmgkbrs1064796845
gwascentralrs1064796845
openSNPrs1064796845
23andMers1064796845
23andMe allrs1064796845
SNPshotrs1064796845
SNPdbers1064796845
MSV3drs1064796845
GWAS Ctlgrs1064796845
Max Magnitude0
ClinVar
Risk rs1064796845(G;G)
Alt rs1064796845(G;G)
Reference Rs1064796845(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22263458C>G
CLNSRC
CLNACC RCV000478394.1,