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rs1064793461

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position22178315
GenePHEX
is asnp
is mentioned by
dbSNPrs1064793461
dbSNP (classic)rs1064793461
ClinGenrs1064793461
ebirs1064793461
HLIrs1064793461
Exacrs1064793461
Gnomadrs1064793461
Varsomers1064793461
LitVarrs1064793461
Maprs1064793461
PheGenIrs1064793461
Biobankrs1064793461
1000 genomesrs1064793461
hgdprs1064793461
ensemblrs1064793461
geneviewrs1064793461
scholarrs1064793461
googlers1064793461
pharmgkbrs1064793461
gwascentralrs1064793461
openSNPrs1064793461
23andMers1064793461
SNPshotrs1064793461
SNPdbers1064793461
MSV3drs1064793461
GWAS Ctlgrs1064793461
Max Magnitude0
ClinVar
Risk rs1064793461(-;-)
Alt rs1064793461(-;-)
Reference Rs1064793461(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22196432delA
CLNSRC
CLNACC RCV000483977.1,