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rs796052834

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796052834(-;C)
Make rs796052834(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100406645
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052834
ClinGenrs796052834
ebirs796052834
HLIrs796052834
Exacrs796052834
Varsomers796052834
Maprs796052834
PheGenIrs796052834
hapmaprs796052834
1000 genomesrs796052834
hgdprs796052834
ensemblrs796052834
gopubmedrs796052834
geneviewrs796052834
scholarrs796052834
googlers796052834
pharmgkbrs796052834
gwascentralrs796052834
openSNPrs796052834
23andMers796052834
23andMe allrs796052834
SNP Nexus

SNPshotrs796052834
SNPdbers796052834
MSV3drs796052834
GWAS Ctlgrs796052834
Max Magnitude0
ClinVar
Risk rs796052834(C;C)
Alt rs796052834(C;C)
Reference Rs796052834(;)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99661644dupG
CLNSRC
CLNACC RCV000188395.1,