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rs796052826

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052826(-;-)
Make rs796052826(-;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100408074
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052826
dbSNP (classic)rs796052826
ClinGenrs796052826
ebirs796052826
HLIrs796052826
Exacrs796052826
Gnomadrs796052826
Varsomers796052826
LitVarrs796052826
Maprs796052826
PheGenIrs796052826
Biobankrs796052826
1000 genomesrs796052826
hgdprs796052826
ensemblrs796052826
geneviewrs796052826
scholarrs796052826
googlers796052826
pharmgkbrs796052826
gwascentralrs796052826
openSNPrs796052826
23andMers796052826
SNPshotrs796052826
SNPdbers796052826
MSV3drs796052826
GWAS Ctlgrs796052826
Max Magnitude0
ClinVar
Risk rs796052826(-;-)
Alt rs796052826(-;-)
Reference Rs796052826(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663072delC
CLNSRC
CLNACC RCV000188386.1,