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rs1057517797

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517797(C;C)
Make rs1057517797(C;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22227616
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1057517797
dbSNP (old)rs1057517797
ClinGenrs1057517797
ebirs1057517797
HLIrs1057517797
Exacrs1057517797
Gnomadrs1057517797
Varsomers1057517797
Maprs1057517797
PheGenIrs1057517797
Biobankrs1057517797
1000 genomesrs1057517797
hgdprs1057517797
ensemblrs1057517797
gopubmedrs1057517797
geneviewrs1057517797
scholarrs1057517797
googlers1057517797
pharmgkbrs1057517797
gwascentralrs1057517797
openSNPrs1057517797
23andMers1057517797
23andMe allrs1057517797
SNPshotrs1057517797
SNPdbers1057517797
MSV3drs1057517797
GWAS Ctlgrs1057517797
Max Magnitude0
ClinVar
Risk rs1057517797(C;C)
Alt rs1057517797(C;C)
Reference Rs1057517797(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22245733G>C
CLNSRC
CLNACC RCV000413865.1,