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rs796052833

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTACCTGG;CTACCTGG) 0 common in clinvar
Make rs796052833(-;-)
Make rs796052833(-;CTACCTGG)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100406839
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052833
dbSNP (old)rs796052833
ClinGenrs796052833
ebirs796052833
HLIrs796052833
Exacrs796052833
Gnomadrs796052833
Varsomers796052833
Maprs796052833
PheGenIrs796052833
Biobankrs796052833
1000 genomesrs796052833
hgdprs796052833
ensemblrs796052833
gopubmedrs796052833
geneviewrs796052833
scholarrs796052833
googlers796052833
pharmgkbrs796052833
gwascentralrs796052833
openSNPrs796052833
23andMers796052833
23andMe allrs796052833
SNP Nexus

SNPshotrs796052833
SNPdbers796052833
MSV3drs796052833
GWAS Ctlgrs796052833
Max Magnitude0
ClinVar
Risk rs796052833(-;-)
Alt rs796052833(-;-)
Reference Rs796052833(CTACCTGG;CTACCTGG)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99661837_99661844delCCAGGTAG
CLNSRC
CLNACC RCV000188394.1,