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rs796052797

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052797(G;T)
Make rs796052797(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100408228
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052797
ebirs796052797
HLIrs796052797
Exacrs796052797
Varsomers796052797
Maprs796052797
PheGenIrs796052797
hapmaprs796052797
1000 genomesrs796052797
hgdprs796052797
ensemblrs796052797
gopubmedrs796052797
geneviewrs796052797
scholarrs796052797
googlers796052797
pharmgkbrs796052797
gwascentralrs796052797
openSNPrs796052797
23andMers796052797
23andMe allrs796052797
SNP Nexus

SNPshotrs796052797
SNPdbers796052797
MSV3drs796052797
GWAS Ctlgrs796052797
Max Magnitude0
ClinVar
Risk rs796052797(T;T)
Alt rs796052797(T;T)
Reference rs796052797(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663226C>A
CLNSRC
CLNACC RCV000188347.2,