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rs1064795511

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position100408470
GenePCDH19
is asnp
is mentioned by
dbSNPrs1064795511
dbSNP (old)rs1064795511
ClinGenrs1064795511
ebirs1064795511
HLIrs1064795511
Exacrs1064795511
Gnomadrs1064795511
Varsomers1064795511
Maprs1064795511
PheGenIrs1064795511
Biobankrs1064795511
1000 genomesrs1064795511
hgdprs1064795511
ensemblrs1064795511
gopubmedrs1064795511
geneviewrs1064795511
scholarrs1064795511
googlers1064795511
pharmgkbrs1064795511
gwascentralrs1064795511
openSNPrs1064795511
23andMers1064795511
23andMe allrs1064795511
SNPshotrs1064795511
SNPdbers1064795511
MSV3drs1064795511
GWAS Ctlgrs1064795511
Max Magnitude0
ClinVar
Risk rs1064795511(T;T)
Alt rs1064795511(T;T)
Reference Rs1064795511(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663468G>A
CLNSRC
CLNACC RCV000478041.1,