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rs796052811

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052811(C;T)
Make rs796052811(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100407567
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052811
ebirs796052811
HLIrs796052811
Exacrs796052811
Varsomers796052811
Maprs796052811
PheGenIrs796052811
hapmaprs796052811
1000 genomesrs796052811
hgdprs796052811
ensemblrs796052811
gopubmedrs796052811
geneviewrs796052811
scholarrs796052811
googlers796052811
pharmgkbrs796052811
gwascentralrs796052811
openSNPrs796052811
23andMers796052811
23andMe allrs796052811
SNP Nexus

SNPshotrs796052811
SNPdbers796052811
MSV3drs796052811
GWAS Ctlgrs796052811
Max Magnitude0
ClinVar
Risk rs796052811(T;T)
Alt rs796052811(T;T)
Reference rs796052811(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662565G>A
CLNSRC
CLNACC RCV000188363.1,