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rs796052839

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052839(A;G)
Make rs796052839(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100407579
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052839
ebirs796052839
HLIrs796052839
Exacrs796052839
Varsomers796052839
Maprs796052839
PheGenIrs796052839
hapmaprs796052839
1000 genomesrs796052839
hgdprs796052839
ensemblrs796052839
gopubmedrs796052839
geneviewrs796052839
scholarrs796052839
googlers796052839
pharmgkbrs796052839
gwascentralrs796052839
openSNPrs796052839
23andMers796052839
23andMe allrs796052839
SNP Nexus

SNPshotrs796052839
SNPdbers796052839
MSV3drs796052839
GWAS Ctlgrs796052839
Max Magnitude0
ClinVar
Risk rs796052839(G;G)
Alt rs796052839(G;G)
Reference rs796052839(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662577T>C
CLNSRC
CLNACC RCV000188401.2,