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rs1057517791

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517791(-;-)
Make rs1057517791(-;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22096988
GenePHEX
is asnp
is mentioned by
dbSNPrs1057517791
dbSNP (old)rs1057517791
ClinGenrs1057517791
ebirs1057517791
HLIrs1057517791
Exacrs1057517791
Gnomadrs1057517791
Varsomers1057517791
Maprs1057517791
PheGenIrs1057517791
Biobankrs1057517791
1000 genomesrs1057517791
hgdprs1057517791
ensemblrs1057517791
gopubmedrs1057517791
geneviewrs1057517791
scholarrs1057517791
googlers1057517791
pharmgkbrs1057517791
gwascentralrs1057517791
openSNPrs1057517791
23andMers1057517791
23andMe allrs1057517791
SNPshotrs1057517791
SNPdbers1057517791
MSV3drs1057517791
GWAS Ctlgrs1057517791
Max Magnitude0
ClinVar
Risk rs1057517791(-;-)
Alt rs1057517791(-;-)
Reference Rs1057517791(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22115106delG
CLNSRC
CLNACC RCV000413674.1,