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rs1064795834

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position100408506
GenePCDH19
is asnp
is mentioned by
dbSNPrs1064795834
dbSNP (old)rs1064795834
ClinGenrs1064795834
ebirs1064795834
HLIrs1064795834
Exacrs1064795834
Gnomadrs1064795834
Varsomers1064795834
Maprs1064795834
PheGenIrs1064795834
Biobankrs1064795834
1000 genomesrs1064795834
hgdprs1064795834
ensemblrs1064795834
gopubmedrs1064795834
geneviewrs1064795834
scholarrs1064795834
googlers1064795834
pharmgkbrs1064795834
gwascentralrs1064795834
openSNPrs1064795834
23andMers1064795834
23andMe allrs1064795834
SNPshotrs1064795834
SNPdbers1064795834
MSV3drs1064795834
GWAS Ctlgrs1064795834
Max Magnitude0
ClinVar
Risk rs1064795834(T;T)
Alt rs1064795834(T;T)
Reference Rs1064795834(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663504T>A
CLNSRC
CLNACC RCV000485018.1,