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rs796052822

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052822(A;G)
Make rs796052822(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100406725
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052822
ebirs796052822
HLIrs796052822
Exacrs796052822
Varsomers796052822
Maprs796052822
PheGenIrs796052822
hapmaprs796052822
1000 genomesrs796052822
hgdprs796052822
ensemblrs796052822
gopubmedrs796052822
geneviewrs796052822
scholarrs796052822
googlers796052822
pharmgkbrs796052822
gwascentralrs796052822
openSNPrs796052822
23andMers796052822
23andMe allrs796052822
SNP Nexus

SNPshotrs796052822
SNPdbers796052822
MSV3drs796052822
GWAS Ctlgrs796052822
Max Magnitude0
ClinVar
Risk rs796052822(G;G)
Alt rs796052822(G;G)
Reference rs796052822(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99661723T>C
CLNSRC
CLNACC RCV000188377.2,