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rs1064795147

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position22227506
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1064795147
dbSNP (old)rs1064795147
ClinGenrs1064795147
ebirs1064795147
HLIrs1064795147
Exacrs1064795147
Gnomadrs1064795147
Varsomers1064795147
Maprs1064795147
PheGenIrs1064795147
Biobankrs1064795147
1000 genomesrs1064795147
hgdprs1064795147
ensemblrs1064795147
gopubmedrs1064795147
geneviewrs1064795147
scholarrs1064795147
googlers1064795147
pharmgkbrs1064795147
gwascentralrs1064795147
openSNPrs1064795147
23andMers1064795147
23andMe allrs1064795147
SNPshotrs1064795147
SNPdbers1064795147
MSV3drs1064795147
GWAS Ctlgrs1064795147
Max Magnitude0
ClinVar
Risk rs1064795147(C;C)
Alt rs1064795147(C;C)
Reference Rs1064795147(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22245623G>C
CLNSRC
CLNACC RCV000482606.1,