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rs1057521800

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521800(A;G)
Make rs1057521800(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22219074
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1057521800
dbSNP (old)rs1057521800
ClinGenrs1057521800
ebirs1057521800
HLIrs1057521800
Exacrs1057521800
Gnomadrs1057521800
Varsomers1057521800
Maprs1057521800
PheGenIrs1057521800
Biobankrs1057521800
1000 genomesrs1057521800
hgdprs1057521800
ensemblrs1057521800
gopubmedrs1057521800
geneviewrs1057521800
scholarrs1057521800
googlers1057521800
pharmgkbrs1057521800
gwascentralrs1057521800
openSNPrs1057521800
23andMers1057521800
23andMe allrs1057521800
SNPshotrs1057521800
SNPdbers1057521800
MSV3drs1057521800
GWAS Ctlgrs1057521800
Max Magnitude0
ClinVar
Risk rs1057521800(G;G)
Alt rs1057521800(G;G)
Reference Rs1057521800(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22237191A>G
CLNSRC
CLNACC RCV000444535.1,