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rs1064796942

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position22111534
GenePHEX
is asnp
is mentioned by
dbSNPrs1064796942
dbSNP (old)rs1064796942
ClinGenrs1064796942
ebirs1064796942
HLIrs1064796942
Exacrs1064796942
Gnomadrs1064796942
Varsomers1064796942
Maprs1064796942
PheGenIrs1064796942
Biobankrs1064796942
1000 genomesrs1064796942
hgdprs1064796942
ensemblrs1064796942
gopubmedrs1064796942
geneviewrs1064796942
scholarrs1064796942
googlers1064796942
pharmgkbrs1064796942
gwascentralrs1064796942
openSNPrs1064796942
23andMers1064796942
23andMe allrs1064796942
SNPshotrs1064796942
SNPdbers1064796942
MSV3drs1064796942
GWAS Ctlgrs1064796942
Max Magnitude0
ClinVar
Risk rs1064796942(T;T)
Alt rs1064796942(T;T)
Reference Rs1064796942(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22129652C>T
CLNSRC
CLNACC RCV000481323.1,