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rs1057518214

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518214(G;G)
Make rs1057518214(G;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22178382
GenePHEX
is asnp
is mentioned by
dbSNPrs1057518214
dbSNP (classic)rs1057518214
ClinGenrs1057518214
ebirs1057518214
HLIrs1057518214
Exacrs1057518214
Gnomadrs1057518214
Varsomers1057518214
LitVarrs1057518214
Maprs1057518214
PheGenIrs1057518214
Biobankrs1057518214
1000 genomesrs1057518214
hgdprs1057518214
ensemblrs1057518214
geneviewrs1057518214
scholarrs1057518214
googlers1057518214
pharmgkbrs1057518214
gwascentralrs1057518214
openSNPrs1057518214
23andMers1057518214
23andMe allrs1057518214
SNPshotrs1057518214
SNPdbers1057518214
MSV3drs1057518214
GWAS Ctlgrs1057518214
Max Magnitude0
ClinVar
Risk rs1057518214(G;G)
Alt rs1057518214(G;G)
Reference Rs1057518214(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22196499T>G
CLNSRC
CLNACC RCV000412767.1,