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rs1064795949

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(TGT;TGT) 0 common in clinvar
ChromosomeX
Position22047194
GenePHEX
is asnp
is mentioned by
dbSNPrs1064795949
dbSNP (old)rs1064795949
ClinGenrs1064795949
ebirs1064795949
HLIrs1064795949
Exacrs1064795949
Gnomadrs1064795949
Varsomers1064795949
Maprs1064795949
PheGenIrs1064795949
Biobankrs1064795949
1000 genomesrs1064795949
hgdprs1064795949
ensemblrs1064795949
gopubmedrs1064795949
geneviewrs1064795949
scholarrs1064795949
googlers1064795949
pharmgkbrs1064795949
gwascentralrs1064795949
openSNPrs1064795949
23andMers1064795949
23andMe allrs1064795949
SNPshotrs1064795949
SNPdbers1064795949
MSV3drs1064795949
GWAS Ctlgrs1064795949
Max Magnitude0
ClinVar
Risk rs1064795949(-;-)
Alt rs1064795949(-;-)
Reference Rs1064795949(TGT;TGT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22065312_22065314delTTG
CLNSRC
CLNACC RCV000480501.1,