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rs1085307873

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(CTCT;CTCT) 0 common in clinvar
ChromosomeX
Position100407176
GenePCDH19
is asnp
is mentioned by
dbSNPrs1085307873
dbSNP (old)rs1085307873
ClinGenrs1085307873
ebirs1085307873
HLIrs1085307873
Exacrs1085307873
Gnomadrs1085307873
Varsomers1085307873
Maprs1085307873
PheGenIrs1085307873
Biobankrs1085307873
1000 genomesrs1085307873
hgdprs1085307873
ensemblrs1085307873
gopubmedrs1085307873
geneviewrs1085307873
scholarrs1085307873
googlers1085307873
pharmgkbrs1085307873
gwascentralrs1085307873
openSNPrs1085307873
23andMers1085307873
23andMe allrs1085307873
SNPshotrs1085307873
SNPdbers1085307873
MSV3drs1085307873
GWAS Ctlgrs1085307873
Max Magnitude0
ClinVar
Risk rs1085307873(-;-)
Alt rs1085307873(-;-)
Reference Rs1085307873(CTCT;CTCT)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662174_99662177delAGAG
CLNSRC
CLNACC RCV000489321.1,