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rs796052843

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTCT;CTCT) 0 common in clinvar
Make rs796052843(-;-)
Make rs796052843(-;CTCT)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100406639
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052843
ClinGenrs796052843
ebirs796052843
HLIrs796052843
Exacrs796052843
Varsomers796052843
Maprs796052843
PheGenIrs796052843
hapmaprs796052843
1000 genomesrs796052843
hgdprs796052843
ensemblrs796052843
gopubmedrs796052843
geneviewrs796052843
scholarrs796052843
googlers796052843
pharmgkbrs796052843
gwascentralrs796052843
openSNPrs796052843
23andMers796052843
23andMe allrs796052843
SNP Nexus

SNPshotrs796052843
SNPdbers796052843
MSV3drs796052843
GWAS Ctlgrs796052843
Max Magnitude0
ClinVar
Risk rs796052843(-;-)
Alt rs796052843(-;-)
Reference Rs796052843(CTCT;CTCT)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99661637_99661640delAGAG
CLNSRC
CLNACC RCV000188406.1,