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rs796052816

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052816(C;T)
Make rs796052816(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100407247
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052816
ebirs796052816
HLIrs796052816
Exacrs796052816
Varsomers796052816
Maprs796052816
PheGenIrs796052816
hapmaprs796052816
1000 genomesrs796052816
hgdprs796052816
ensemblrs796052816
gopubmedrs796052816
geneviewrs796052816
scholarrs796052816
googlers796052816
pharmgkbrs796052816
gwascentralrs796052816
openSNPrs796052816
23andMers796052816
23andMe allrs796052816
SNP Nexus

SNPshotrs796052816
SNPdbers796052816
MSV3drs796052816
GWAS Ctlgrs796052816
Max Magnitude0
ClinVar
Risk rs796052816(T;T)
Alt rs796052816(T;T)
Reference rs796052816(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662245G>A
CLNSRC
CLNACC RCV000188369.1,