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rs1057517795

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517795(A;A)
Make rs1057517795(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22219050
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1057517795
dbSNP (old)rs1057517795
ClinGenrs1057517795
ebirs1057517795
HLIrs1057517795
Exacrs1057517795
Gnomadrs1057517795
Varsomers1057517795
Maprs1057517795
PheGenIrs1057517795
Biobankrs1057517795
1000 genomesrs1057517795
hgdprs1057517795
ensemblrs1057517795
gopubmedrs1057517795
geneviewrs1057517795
scholarrs1057517795
googlers1057517795
pharmgkbrs1057517795
gwascentralrs1057517795
openSNPrs1057517795
23andMers1057517795
23andMe allrs1057517795
SNPshotrs1057517795
SNPdbers1057517795
MSV3drs1057517795
GWAS Ctlgrs1057517795
Max Magnitude0
ClinVar
Risk rs1057517795(A;A) rs1057517795(T;T)
Alt rs1057517795(A;A) rs1057517795(T;T)
Reference Rs1057517795(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22237167G>A; NC_000023.10:g.22237167G>T
CLNSRC
CLNACC RCV000413745.1, RCV000414654.1,