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rs1064795237

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position100408303
GenePCDH19
is asnp
is mentioned by
dbSNPrs1064795237
dbSNP (old)rs1064795237
ClinGenrs1064795237
ebirs1064795237
HLIrs1064795237
Exacrs1064795237
Gnomadrs1064795237
Varsomers1064795237
Maprs1064795237
PheGenIrs1064795237
Biobankrs1064795237
1000 genomesrs1064795237
hgdprs1064795237
ensemblrs1064795237
gopubmedrs1064795237
geneviewrs1064795237
scholarrs1064795237
googlers1064795237
pharmgkbrs1064795237
gwascentralrs1064795237
openSNPrs1064795237
23andMers1064795237
23andMe allrs1064795237
SNPshotrs1064795237
SNPdbers1064795237
MSV3drs1064795237
GWAS Ctlgrs1064795237
Max Magnitude0
ClinVar
Risk rs1064795237(A;A)
Alt rs1064795237(A;A)
Reference Rs1064795237(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663301A>T
CLNSRC
CLNACC RCV000485618.1,