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rs1057517981

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517981(A;A)
Make rs1057517981(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22247901
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1057517981
dbSNP (old)rs1057517981
ClinGenrs1057517981
ebirs1057517981
HLIrs1057517981
Exacrs1057517981
Gnomadrs1057517981
Varsomers1057517981
Maprs1057517981
PheGenIrs1057517981
Biobankrs1057517981
1000 genomesrs1057517981
hgdprs1057517981
ensemblrs1057517981
gopubmedrs1057517981
geneviewrs1057517981
scholarrs1057517981
googlers1057517981
pharmgkbrs1057517981
gwascentralrs1057517981
openSNPrs1057517981
23andMers1057517981
23andMe allrs1057517981
SNPshotrs1057517981
SNPdbers1057517981
MSV3drs1057517981
GWAS Ctlgrs1057517981
Max Magnitude0
ClinVar
Risk rs1057517981(A;A)
Alt rs1057517981(A;A)
Reference Rs1057517981(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22266018G>A
CLNSRC
CLNACC RCV000413547.1,