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rs796052812

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052812(C;T)
Make rs796052812(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100407484
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052812
ebirs796052812
HLIrs796052812
Exacrs796052812
Varsomers796052812
Maprs796052812
PheGenIrs796052812
hapmaprs796052812
1000 genomesrs796052812
hgdprs796052812
ensemblrs796052812
gopubmedrs796052812
geneviewrs796052812
scholarrs796052812
googlers796052812
pharmgkbrs796052812
gwascentralrs796052812
openSNPrs796052812
23andMers796052812
23andMe allrs796052812
SNP Nexus

SNPshotrs796052812
SNPdbers796052812
MSV3drs796052812
GWAS Ctlgrs796052812
Max Magnitude0
ClinVar
Risk rs796052812(T;T)
Alt rs796052812(T;T)
Reference rs796052812(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662482G>A
CLNSRC
CLNACC RCV000188364.1,