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rs1057517796

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517796(-;T)
Make rs1057517796(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22219105
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1057517796
dbSNP (old)rs1057517796
ClinGenrs1057517796
ebirs1057517796
HLIrs1057517796
Exacrs1057517796
Gnomadrs1057517796
Varsomers1057517796
Maprs1057517796
PheGenIrs1057517796
Biobankrs1057517796
1000 genomesrs1057517796
hgdprs1057517796
ensemblrs1057517796
gopubmedrs1057517796
geneviewrs1057517796
scholarrs1057517796
googlers1057517796
pharmgkbrs1057517796
gwascentralrs1057517796
openSNPrs1057517796
23andMers1057517796
23andMe allrs1057517796
SNPshotrs1057517796
SNPdbers1057517796
MSV3drs1057517796
GWAS Ctlgrs1057517796
Max Magnitude0
ClinVar
Risk rs1057517796(T;T)
Alt rs1057517796(T;T)
Reference Rs1057517796(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22237222dupT
CLNSRC
CLNACC RCV000412973.1,