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rs796052836

From SNPedia

Orientationminus
Make rs796052836(-;-)
Make rs796052836(-;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100402741
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052836
ebirs796052836
HLIrs796052836
Exacrs796052836
Varsomers796052836
Maprs796052836
PheGenIrs796052836
hapmaprs796052836
1000 genomesrs796052836
hgdprs796052836
ensemblrs796052836
gopubmedrs796052836
geneviewrs796052836
scholarrs796052836
googlers796052836
pharmgkbrs796052836
gwascentralrs796052836
openSNPrs796052836
23andMers796052836
23andMe allrs796052836
SNP Nexus

SNPshotrs796052836
SNPdbers796052836
MSV3drs796052836
GWAS Ctlgrs796052836
Max Magnitude
ClinVar
Risk rs796052836(;)
Alt rs796052836(;)
Reference rs796052836(A;A)
Significance Pathogenic
Disease not provided Early infantile epileptic encephalopathy 9
Variation info
Gene PCDH19
CLNDBN not provided Early infantile epileptic encephalopathy 9
Reversed 1
HGVS NC_000023.10:g.99657739delT
CLNSRC
CLNACC RCV000188397.1, RCV000192451.1,