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rs796052814

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052814(A;T)
Make rs796052814(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100407357
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052814
ebirs796052814
HLIrs796052814
Exacrs796052814
Varsomers796052814
Maprs796052814
PheGenIrs796052814
hapmaprs796052814
1000 genomesrs796052814
hgdprs796052814
ensemblrs796052814
gopubmedrs796052814
geneviewrs796052814
scholarrs796052814
googlers796052814
pharmgkbrs796052814
gwascentralrs796052814
openSNPrs796052814
23andMers796052814
23andMe allrs796052814
SNP Nexus

SNPshotrs796052814
SNPdbers796052814
MSV3drs796052814
GWAS Ctlgrs796052814
Max Magnitude0
ClinVar
Risk rs796052814(T;T)
Alt rs796052814(T;T)
Reference rs796052814(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662355T>A
CLNSRC
CLNACC RCV000188367.1,