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rs1057518596

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518596(A;A)
Make rs1057518596(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22227612
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1057518596
dbSNP (classic)rs1057518596
ClinGenrs1057518596
ebirs1057518596
HLIrs1057518596
Exacrs1057518596
Gnomadrs1057518596
Varsomers1057518596
LitVarrs1057518596
Maprs1057518596
PheGenIrs1057518596
Biobankrs1057518596
1000 genomesrs1057518596
hgdprs1057518596
ensemblrs1057518596
geneviewrs1057518596
scholarrs1057518596
googlers1057518596
pharmgkbrs1057518596
gwascentralrs1057518596
openSNPrs1057518596
23andMers1057518596
23andMe allrs1057518596
SNPshotrs1057518596
SNPdbers1057518596
MSV3drs1057518596
GWAS Ctlgrs1057518596
Max Magnitude0
ClinVar
Risk rs1057518596(A;A)
Alt rs1057518596(A;A)
Reference Rs1057518596(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22245729G>A
CLNSRC
CLNACC RCV000413408.1,