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rs796052806

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052806(C;C)
Make rs796052806(C;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100407964
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052806
ebirs796052806
HLIrs796052806
Exacrs796052806
Varsomers796052806
Maprs796052806
PheGenIrs796052806
hapmaprs796052806
1000 genomesrs796052806
hgdprs796052806
ensemblrs796052806
gopubmedrs796052806
geneviewrs796052806
scholarrs796052806
googlers796052806
pharmgkbrs796052806
gwascentralrs796052806
openSNPrs796052806
23andMers796052806
23andMe allrs796052806
SNP Nexus

SNPshotrs796052806
SNPdbers796052806
MSV3drs796052806
GWAS Ctlgrs796052806
Max Magnitude0
ClinVar
Risk rs796052806(C;C)
Alt rs796052806(C;C)
Reference rs796052806(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662962C>G
CLNSRC
CLNACC RCV000188356.2,