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rs796052842

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796052842(-;G)
Make rs796052842(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100407631
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052842
ClinGenrs796052842
ebirs796052842
HLIrs796052842
Exacrs796052842
Varsomers796052842
Maprs796052842
PheGenIrs796052842
hapmaprs796052842
1000 genomesrs796052842
hgdprs796052842
ensemblrs796052842
gopubmedrs796052842
geneviewrs796052842
scholarrs796052842
googlers796052842
pharmgkbrs796052842
gwascentralrs796052842
openSNPrs796052842
23andMers796052842
23andMe allrs796052842
SNP Nexus

SNPshotrs796052842
SNPdbers796052842
MSV3drs796052842
GWAS Ctlgrs796052842
Max Magnitude0
ClinVar
Risk rs796052842(G;G)
Alt rs796052842(G;G)
Reference Rs796052842(;)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662630dupC
CLNSRC
CLNACC RCV000188405.1,