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rs1057517980

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517980(G;T)
Make rs1057517980(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22219071
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1057517980
dbSNP (old)rs1057517980
ClinGenrs1057517980
ebirs1057517980
HLIrs1057517980
Exacrs1057517980
Gnomadrs1057517980
Varsomers1057517980
Maprs1057517980
PheGenIrs1057517980
Biobankrs1057517980
1000 genomesrs1057517980
hgdprs1057517980
ensemblrs1057517980
gopubmedrs1057517980
geneviewrs1057517980
scholarrs1057517980
googlers1057517980
pharmgkbrs1057517980
gwascentralrs1057517980
openSNPrs1057517980
23andMers1057517980
23andMe allrs1057517980
SNPshotrs1057517980
SNPdbers1057517980
MSV3drs1057517980
GWAS Ctlgrs1057517980
Max Magnitude0
ClinVar
Risk rs1057517980(A;A) rs1057517980(T;T)
Alt rs1057517980(A;A) rs1057517980(T;T)
Reference Rs1057517980(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22237188G>A; NC_000023.10:g.22237188G>T
CLNSRC
CLNACC RCV000419789.1, RCV000412906.1,