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rs1064794781

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GCAGCTCCA;GCAGCTCCA) 0 common in clinvar
ChromosomeX
Position100342068
GenePCDH19
is asnp
is mentioned by
dbSNPrs1064794781
dbSNP (old)rs1064794781
ClinGenrs1064794781
ebirs1064794781
HLIrs1064794781
Exacrs1064794781
Gnomadrs1064794781
Varsomers1064794781
Maprs1064794781
PheGenIrs1064794781
Biobankrs1064794781
1000 genomesrs1064794781
hgdprs1064794781
ensemblrs1064794781
gopubmedrs1064794781
geneviewrs1064794781
scholarrs1064794781
googlers1064794781
pharmgkbrs1064794781
gwascentralrs1064794781
openSNPrs1064794781
23andMers1064794781
23andMe allrs1064794781
SNPshotrs1064794781
SNPdbers1064794781
MSV3drs1064794781
GWAS Ctlgrs1064794781
Max Magnitude0
ClinVar
Risk rs1064794781(-;-)
Alt rs1064794781(-;-)
Reference Rs1064794781(GCAGCTCCA;GCAGCTCCA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99597066_99597074delTGGAGCTGC
CLNSRC
CLNACC RCV000484556.1,