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rs1057518348

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518348(A;A)
Make rs1057518348(A;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22077704
GenePHEX
is asnp
is mentioned by
dbSNPrs1057518348
dbSNP (old)rs1057518348
ClinGenrs1057518348
ebirs1057518348
HLIrs1057518348
Exacrs1057518348
Gnomadrs1057518348
Varsomers1057518348
Maprs1057518348
PheGenIrs1057518348
Biobankrs1057518348
1000 genomesrs1057518348
hgdprs1057518348
ensemblrs1057518348
gopubmedrs1057518348
geneviewrs1057518348
scholarrs1057518348
googlers1057518348
pharmgkbrs1057518348
gwascentralrs1057518348
openSNPrs1057518348
23andMers1057518348
23andMe allrs1057518348
SNPshotrs1057518348
SNPdbers1057518348
MSV3drs1057518348
GWAS Ctlgrs1057518348
Max Magnitude0
ClinVar
Risk rs1057518348(A;A)
Alt rs1057518348(A;A)
Reference Rs1057518348(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22095822T>A
CLNSRC
CLNACC RCV000413368.1,