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rs1057518377

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518377(A;A)
Make rs1057518377(A;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22178378
GenePHEX
is asnp
is mentioned by
dbSNPrs1057518377
dbSNP (classic)rs1057518377
ClinGenrs1057518377
ebirs1057518377
HLIrs1057518377
Exacrs1057518377
Gnomadrs1057518377
Varsomers1057518377
LitVarrs1057518377
Maprs1057518377
PheGenIrs1057518377
Biobankrs1057518377
1000 genomesrs1057518377
hgdprs1057518377
ensemblrs1057518377
geneviewrs1057518377
scholarrs1057518377
googlers1057518377
pharmgkbrs1057518377
gwascentralrs1057518377
openSNPrs1057518377
23andMers1057518377
23andMe allrs1057518377
SNPshotrs1057518377
SNPdbers1057518377
MSV3drs1057518377
GWAS Ctlgrs1057518377
Max Magnitude0
ClinVar
Risk rs1057518377(A;A)
Alt rs1057518377(A;A)
Reference Rs1057518377(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22196495T>A
CLNSRC
CLNACC RCV000414411.1,