Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057517800

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs1057517800(-;-)
Make rs1057517800(-;CT)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position22247947
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs1057517800
dbSNP (classic)rs1057517800
ClinGenrs1057517800
ebirs1057517800
HLIrs1057517800
Exacrs1057517800
Gnomadrs1057517800
Varsomers1057517800
LitVarrs1057517800
Maprs1057517800
PheGenIrs1057517800
Biobankrs1057517800
1000 genomesrs1057517800
hgdprs1057517800
ensemblrs1057517800
geneviewrs1057517800
scholarrs1057517800
googlers1057517800
pharmgkbrs1057517800
gwascentralrs1057517800
openSNPrs1057517800
23andMers1057517800
23andMe allrs1057517800
SNPshotrs1057517800
SNPdbers1057517800
MSV3drs1057517800
GWAS Ctlgrs1057517800
Max Magnitude0
ClinVar
Risk rs1057517800(-;-)
Alt rs1057517800(-;-)
Reference Rs1057517800(CT;CT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22266064_22266065delCT
CLNSRC
CLNACC RCV000413761.1,