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rs1064796928

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position22178377
GenePHEX
is asnp
is mentioned by
dbSNPrs1064796928
dbSNP (classic)rs1064796928
ClinGenrs1064796928
ebirs1064796928
HLIrs1064796928
Exacrs1064796928
Gnomadrs1064796928
Varsomers1064796928
LitVarrs1064796928
Maprs1064796928
PheGenIrs1064796928
Biobankrs1064796928
1000 genomesrs1064796928
hgdprs1064796928
ensemblrs1064796928
geneviewrs1064796928
scholarrs1064796928
googlers1064796928
pharmgkbrs1064796928
gwascentralrs1064796928
openSNPrs1064796928
23andMers1064796928
23andMe allrs1064796928
SNPshotrs1064796928
SNPdbers1064796928
MSV3drs1064796928
GWAS Ctlgrs1064796928
Max Magnitude0
ClinVar
Risk rs1064796928(T;T)
Alt rs1064796928(T;T)
Reference Rs1064796928(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22196494G>T
CLNSRC
CLNACC RCV000486596.1,