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rs1057524608

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524608(G;T)
Make rs1057524608(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22219108
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1057524608
dbSNP (old)rs1057524608
ClinGenrs1057524608
ebirs1057524608
HLIrs1057524608
Exacrs1057524608
Gnomadrs1057524608
Varsomers1057524608
LitVarrs1057524608
Maprs1057524608
PheGenIrs1057524608
Biobankrs1057524608
1000 genomesrs1057524608
hgdprs1057524608
ensemblrs1057524608
gopubmedrs1057524608
geneviewrs1057524608
scholarrs1057524608
googlers1057524608
pharmgkbrs1057524608
gwascentralrs1057524608
openSNPrs1057524608
23andMers1057524608
23andMe allrs1057524608
SNPshotrs1057524608
SNPdbers1057524608
MSV3drs1057524608
GWAS Ctlgrs1057524608
Max Magnitude0
ClinVar
Risk rs1057524608(T;T)
Alt rs1057524608(T;T)
Reference Rs1057524608(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22237225G>T
CLNSRC
CLNACC RCV000419875.1,