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rs1057517789

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517789(A;A)
Make rs1057517789(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22077539
GenePHEX
is asnp
is mentioned by
dbSNPrs1057517789
dbSNP (old)rs1057517789
ClinGenrs1057517789
ebirs1057517789
HLIrs1057517789
Exacrs1057517789
Gnomadrs1057517789
Varsomers1057517789
LitVarrs1057517789
Maprs1057517789
PheGenIrs1057517789
Biobankrs1057517789
1000 genomesrs1057517789
hgdprs1057517789
ensemblrs1057517789
gopubmedrs1057517789
geneviewrs1057517789
scholarrs1057517789
googlers1057517789
pharmgkbrs1057517789
gwascentralrs1057517789
openSNPrs1057517789
23andMers1057517789
23andMe allrs1057517789
SNPshotrs1057517789
SNPdbers1057517789
MSV3drs1057517789
GWAS Ctlgrs1057517789
Max Magnitude0
ClinVar
Risk rs1057517789(A;A)
Alt rs1057517789(A;A)
Reference Rs1057517789(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22095657G>A
CLNSRC
CLNACC RCV000413519.1,