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rs796052801

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052801(C;G)
Make rs796052801(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100408125
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052801
ebirs796052801
HLIrs796052801
Exacrs796052801
Varsomers796052801
Maprs796052801
PheGenIrs796052801
hapmaprs796052801
1000 genomesrs796052801
hgdprs796052801
ensemblrs796052801
gopubmedrs796052801
geneviewrs796052801
scholarrs796052801
googlers796052801
pharmgkbrs796052801
gwascentralrs796052801
openSNPrs796052801
23andMers796052801
23andMe allrs796052801
SNP Nexus

SNPshotrs796052801
SNPdbers796052801
MSV3drs796052801
GWAS Ctlgrs796052801
Max Magnitude0
ClinVar
Risk rs796052801(G;G)
Alt rs796052801(G;G)
Reference rs796052801(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663123G>C
CLNSRC
CLNACC RCV000188351.1,