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rs1064794762

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position100407226
GenePCDH19
is asnp
is mentioned by
dbSNPrs1064794762
dbSNP (classic)rs1064794762
ClinGenrs1064794762
ebirs1064794762
HLIrs1064794762
Exacrs1064794762
Gnomadrs1064794762
Varsomers1064794762
LitVarrs1064794762
Maprs1064794762
PheGenIrs1064794762
Biobankrs1064794762
1000 genomesrs1064794762
hgdprs1064794762
ensemblrs1064794762
geneviewrs1064794762
scholarrs1064794762
googlers1064794762
pharmgkbrs1064794762
gwascentralrs1064794762
openSNPrs1064794762
23andMers1064794762
23andMe allrs1064794762
SNPshotrs1064794762
SNPdbers1064794762
MSV3drs1064794762
GWAS Ctlgrs1064794762
Max Magnitude0
ClinVar
Risk rs1064794762(C;C)
Alt rs1064794762(C;C)
Reference Rs1064794762(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662224A>G
CLNSRC
CLNACC RCV000485418.1,