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rs796052798

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052798(C;C)
Make rs796052798(C;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100408174
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052798
ebirs796052798
HLIrs796052798
Exacrs796052798
Varsomers796052798
Maprs796052798
PheGenIrs796052798
hapmaprs796052798
1000 genomesrs796052798
hgdprs796052798
ensemblrs796052798
gopubmedrs796052798
geneviewrs796052798
scholarrs796052798
googlers796052798
pharmgkbrs796052798
gwascentralrs796052798
openSNPrs796052798
23andMers796052798
23andMe allrs796052798
SNP Nexus

SNPshotrs796052798
SNPdbers796052798
MSV3drs796052798
GWAS Ctlgrs796052798
Max Magnitude0
ClinVar
Risk rs796052798(C;C)
Alt rs796052798(C;C)
Reference rs796052798(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663172C>G
CLNSRC
CLNACC RCV000188348.1,