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rs796052819

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052819(C;G)
Make rs796052819(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100406916
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052819
ebirs796052819
HLIrs796052819
Exacrs796052819
Varsomers796052819
Maprs796052819
PheGenIrs796052819
hapmaprs796052819
1000 genomesrs796052819
hgdprs796052819
ensemblrs796052819
gopubmedrs796052819
geneviewrs796052819
scholarrs796052819
googlers796052819
pharmgkbrs796052819
gwascentralrs796052819
openSNPrs796052819
23andMers796052819
23andMe allrs796052819
SNP Nexus

SNPshotrs796052819
SNPdbers796052819
MSV3drs796052819
GWAS Ctlgrs796052819
Max Magnitude0
ClinVar
Risk rs796052819(G;G)
Alt rs796052819(G;G)
Reference rs796052819(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99661914G>C
CLNSRC
CLNACC RCV000188374.1,