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rs1057517792

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517792(-;A)
Make rs1057517792(A;A)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22099118
GenePHEX
is asnp
is mentioned by
dbSNPrs1057517792
dbSNP (old)rs1057517792
ClinGenrs1057517792
ebirs1057517792
HLIrs1057517792
Exacrs1057517792
Gnomadrs1057517792
Varsomers1057517792
LitVarrs1057517792
Maprs1057517792
PheGenIrs1057517792
Biobankrs1057517792
1000 genomesrs1057517792
hgdprs1057517792
ensemblrs1057517792
gopubmedrs1057517792
geneviewrs1057517792
scholarrs1057517792
googlers1057517792
pharmgkbrs1057517792
gwascentralrs1057517792
openSNPrs1057517792
23andMers1057517792
23andMe allrs1057517792
SNPshotrs1057517792
SNPdbers1057517792
MSV3drs1057517792
GWAS Ctlgrs1057517792
Max Magnitude0
ClinVar
Risk rs1057517792(A;A)
Alt rs1057517792(A;A)
Reference Rs1057517792(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22117236dupA
CLNSRC
CLNACC RCV000414311.1,