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rs1064796391

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TGG;TGG) 0 common in clinvar
ChromosomeX
Position22094011
GenePHEX
is asnp
is mentioned by
dbSNPrs1064796391
dbSNP (classic)rs1064796391
ClinGenrs1064796391
ebirs1064796391
HLIrs1064796391
Exacrs1064796391
Gnomadrs1064796391
Varsomers1064796391
LitVarrs1064796391
Maprs1064796391
PheGenIrs1064796391
Biobankrs1064796391
1000 genomesrs1064796391
hgdprs1064796391
ensemblrs1064796391
geneviewrs1064796391
scholarrs1064796391
googlers1064796391
pharmgkbrs1064796391
gwascentralrs1064796391
openSNPrs1064796391
23andMers1064796391
23andMe allrs1064796391
SNPshotrs1064796391
SNPdbers1064796391
MSV3drs1064796391
GWAS Ctlgrs1064796391
Max Magnitude0
ClinVar
Risk rs1064796391(-;-)
Alt rs1064796391(-;-)
Reference Rs1064796391(TGG;TGG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22112129_22112131delTGG
CLNSRC
CLNACC RCV000480929.1,