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rs1064797377

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TTTC;TTTC) 0 common in clinvar
ChromosomeX
Position100407730
GenePCDH19
is asnp
is mentioned by
dbSNPrs1064797377
dbSNP (classic)rs1064797377
ClinGenrs1064797377
ebirs1064797377
HLIrs1064797377
Exacrs1064797377
Gnomadrs1064797377
Varsomers1064797377
LitVarrs1064797377
Maprs1064797377
PheGenIrs1064797377
Biobankrs1064797377
1000 genomesrs1064797377
hgdprs1064797377
ensemblrs1064797377
geneviewrs1064797377
scholarrs1064797377
googlers1064797377
pharmgkbrs1064797377
gwascentralrs1064797377
openSNPrs1064797377
23andMers1064797377
23andMe allrs1064797377
SNPshotrs1064797377
SNPdbers1064797377
MSV3drs1064797377
GWAS Ctlgrs1064797377
Max Magnitude0
ClinVar
Risk rs1064797377(-;-)
Alt rs1064797377(-;-)
Reference Rs1064797377(TTTC;TTTC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662728_99662731delGAAA
CLNSRC
CLNACC RCV000487680.1,