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rs1057517896

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517896(C;C)
Make rs1057517896(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22111562
GenePHEX
is asnp
is mentioned by
dbSNPrs1057517896
dbSNP (old)rs1057517896
ClinGenrs1057517896
ebirs1057517896
HLIrs1057517896
Exacrs1057517896
Gnomadrs1057517896
Varsomers1057517896
Maprs1057517896
PheGenIrs1057517896
Biobankrs1057517896
1000 genomesrs1057517896
hgdprs1057517896
ensemblrs1057517896
gopubmedrs1057517896
geneviewrs1057517896
scholarrs1057517896
googlers1057517896
pharmgkbrs1057517896
gwascentralrs1057517896
openSNPrs1057517896
23andMers1057517896
23andMe allrs1057517896
SNPshotrs1057517896
SNPdbers1057517896
MSV3drs1057517896
GWAS Ctlgrs1057517896
Max Magnitude0
ClinVar
Risk rs1057517896(C;C)
Alt rs1057517896(C;C)
Reference Rs1057517896(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22129680T>C
CLNSRC
CLNACC RCV000412709.1,