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rs796052841

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796052841(-;G)
Make rs796052841(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100408379
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052841
ClinGenrs796052841
ebirs796052841
HLIrs796052841
Exacrs796052841
Varsomers796052841
Maprs796052841
PheGenIrs796052841
hapmaprs796052841
1000 genomesrs796052841
hgdprs796052841
ensemblrs796052841
gopubmedrs796052841
geneviewrs796052841
scholarrs796052841
googlers796052841
pharmgkbrs796052841
gwascentralrs796052841
openSNPrs796052841
23andMers796052841
23andMe allrs796052841
SNP Nexus

SNPshotrs796052841
SNPdbers796052841
MSV3drs796052841
GWAS Ctlgrs796052841
Max Magnitude0
ClinVar
Risk rs796052841(G;G)
Alt rs796052841(G;G)
Reference Rs796052841(;)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663377_99663378insC
CLNSRC
CLNACC RCV000188404.1,