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rs796052794

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052794(G;T)
Make rs796052794(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100408507
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052794
ebirs796052794
HLIrs796052794
Exacrs796052794
Varsomers796052794
Maprs796052794
PheGenIrs796052794
hapmaprs796052794
1000 genomesrs796052794
hgdprs796052794
ensemblrs796052794
gopubmedrs796052794
geneviewrs796052794
scholarrs796052794
googlers796052794
pharmgkbrs796052794
gwascentralrs796052794
openSNPrs796052794
23andMers796052794
23andMe allrs796052794
SNP Nexus

SNPshotrs796052794
SNPdbers796052794
MSV3drs796052794
GWAS Ctlgrs796052794
Max Magnitude0
ClinVar
Risk rs796052794(T;T)
Alt rs796052794(T;T)
Reference rs796052794(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663505C>A
CLNSRC
CLNACC RCV000188342.1,