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rs796052817

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052817(C;G)
Make rs796052817(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100406973
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052817
ebirs796052817
HLIrs796052817
Exacrs796052817
Varsomers796052817
Maprs796052817
PheGenIrs796052817
hapmaprs796052817
1000 genomesrs796052817
hgdprs796052817
ensemblrs796052817
gopubmedrs796052817
geneviewrs796052817
scholarrs796052817
googlers796052817
pharmgkbrs796052817
gwascentralrs796052817
openSNPrs796052817
23andMers796052817
23andMe allrs796052817
SNP Nexus

SNPshotrs796052817
SNPdbers796052817
MSV3drs796052817
GWAS Ctlgrs796052817
Max Magnitude0
ClinVar
Risk rs796052817(G;G)
Alt rs796052817(G;G)
Reference rs796052817(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99661971G>C
CLNSRC
CLNACC RCV000188372.1,