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rs796052835

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796052835(-;CT)
Make rs796052835(CT;CT)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100406638
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052835
ClinGenrs796052835
ebirs796052835
HLIrs796052835
Exacrs796052835
Varsomers796052835
Maprs796052835
PheGenIrs796052835
hapmaprs796052835
1000 genomesrs796052835
hgdprs796052835
ensemblrs796052835
gopubmedrs796052835
geneviewrs796052835
scholarrs796052835
googlers796052835
pharmgkbrs796052835
gwascentralrs796052835
openSNPrs796052835
23andMers796052835
23andMe allrs796052835
SNP Nexus

SNPshotrs796052835
SNPdbers796052835
MSV3drs796052835
GWAS Ctlgrs796052835
Max Magnitude0
ClinVar
Risk rs796052835(CT;CT)
Alt rs796052835(CT;CT)
Reference Rs796052835(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99661637_99661638dupAG
CLNSRC
CLNACC RCV000188396.1,