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rs1064794763

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position100407163
GenePCDH19
is asnp
is mentioned by
dbSNPrs1064794763
dbSNP (classic)rs1064794763
ClinGenrs1064794763
ebirs1064794763
HLIrs1064794763
Exacrs1064794763
Gnomadrs1064794763
Varsomers1064794763
LitVarrs1064794763
Maprs1064794763
PheGenIrs1064794763
Biobankrs1064794763
1000 genomesrs1064794763
hgdprs1064794763
ensemblrs1064794763
geneviewrs1064794763
scholarrs1064794763
googlers1064794763
pharmgkbrs1064794763
gwascentralrs1064794763
openSNPrs1064794763
23andMers1064794763
23andMe allrs1064794763
SNPshotrs1064794763
SNPdbers1064794763
MSV3drs1064794763
GWAS Ctlgrs1064794763
Max Magnitude0
ClinVar
Risk rs1064794763(A;A)
Alt rs1064794763(A;A)
Reference Rs1064794763(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662161C>T
CLNSRC
CLNACC RCV000479158.1,