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rs1064796927

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position22114456
GenePHEX
is asnp
is mentioned by
dbSNPrs1064796927
dbSNP (old)rs1064796927
ClinGenrs1064796927
ebirs1064796927
HLIrs1064796927
Exacrs1064796927
Gnomadrs1064796927
Varsomers1064796927
LitVarrs1064796927
Maprs1064796927
PheGenIrs1064796927
Biobankrs1064796927
1000 genomesrs1064796927
hgdprs1064796927
ensemblrs1064796927
gopubmedrs1064796927
geneviewrs1064796927
scholarrs1064796927
googlers1064796927
pharmgkbrs1064796927
gwascentralrs1064796927
openSNPrs1064796927
23andMers1064796927
23andMe allrs1064796927
SNPshotrs1064796927
SNPdbers1064796927
MSV3drs1064796927
GWAS Ctlgrs1064796927
Max Magnitude0
ClinVar
Risk rs1064796927(G;G)
Alt rs1064796927(G;G)
Reference Rs1064796927(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22132574A>G
CLNSRC
CLNACC RCV000482906.1,