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rs1057517799

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517799(G;T)
Make rs1057517799(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22247940
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1057517799
dbSNP (old)rs1057517799
ClinGenrs1057517799
ebirs1057517799
HLIrs1057517799
Exacrs1057517799
Gnomadrs1057517799
Varsomers1057517799
Maprs1057517799
PheGenIrs1057517799
Biobankrs1057517799
1000 genomesrs1057517799
hgdprs1057517799
ensemblrs1057517799
gopubmedrs1057517799
geneviewrs1057517799
scholarrs1057517799
googlers1057517799
pharmgkbrs1057517799
gwascentralrs1057517799
openSNPrs1057517799
23andMers1057517799
23andMe allrs1057517799
SNPshotrs1057517799
SNPdbers1057517799
MSV3drs1057517799
GWAS Ctlgrs1057517799
Max Magnitude0
ClinVar
Risk rs1057517799(T;T)
Alt rs1057517799(T;T)
Reference Rs1057517799(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22266057G>T
CLNSRC
CLNACC RCV000413405.1,