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rs796052813

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052813(G;T)
Make rs796052813(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100407358
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052813
ebirs796052813
HLIrs796052813
Exacrs796052813
Varsomers796052813
Maprs796052813
PheGenIrs796052813
hapmaprs796052813
1000 genomesrs796052813
hgdprs796052813
ensemblrs796052813
gopubmedrs796052813
geneviewrs796052813
scholarrs796052813
googlers796052813
pharmgkbrs796052813
gwascentralrs796052813
openSNPrs796052813
23andMers796052813
23andMe allrs796052813
SNP Nexus

SNPshotrs796052813
SNPdbers796052813
MSV3drs796052813
GWAS Ctlgrs796052813
Max Magnitude0
ClinVar
Risk rs796052813(T;T)
Alt rs796052813(T;T)
Reference rs796052813(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662356C>A
CLNSRC
CLNACC RCV000188366.1,