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rs796052799

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052799(C;G)
Make rs796052799(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100408161
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052799
ebirs796052799
HLIrs796052799
Exacrs796052799
Varsomers796052799
Maprs796052799
PheGenIrs796052799
hapmaprs796052799
1000 genomesrs796052799
hgdprs796052799
ensemblrs796052799
gopubmedrs796052799
geneviewrs796052799
scholarrs796052799
googlers796052799
pharmgkbrs796052799
gwascentralrs796052799
openSNPrs796052799
23andMers796052799
23andMe allrs796052799
SNP Nexus

SNPshotrs796052799
SNPdbers796052799
MSV3drs796052799
GWAS Ctlgrs796052799
Max Magnitude0
ClinVar
Risk rs796052799(G;G)
Alt rs796052799(G;G)
Reference rs796052799(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663159G>C
CLNSRC
CLNACC RCV000188349.2,