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rs796052832

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GGTCATCACAGCCC;GGTCATCACAGCCC) 0 common in clinvar
Make rs796052832(-;-)
Make rs796052832(-;GGTCATCACAGCCC)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100406902
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052832
dbSNP (old)rs796052832
ClinGenrs796052832
ebirs796052832
HLIrs796052832
Exacrs796052832
Gnomadrs796052832
Varsomers796052832
Maprs796052832
PheGenIrs796052832
Biobankrs796052832
1000 genomesrs796052832
hgdprs796052832
ensemblrs796052832
gopubmedrs796052832
geneviewrs796052832
scholarrs796052832
googlers796052832
pharmgkbrs796052832
gwascentralrs796052832
openSNPrs796052832
23andMers796052832
23andMe allrs796052832
SNP Nexus

SNPshotrs796052832
SNPdbers796052832
MSV3drs796052832
GWAS Ctlgrs796052832
Max Magnitude0
ClinVar
Risk rs796052832(-;-)
Alt rs796052832(-;-)
Reference Rs796052832(GGTCATCACAGCCC;GGTCATCACAGCCC)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99661900_99661913delGGGCTGTGATGACC
CLNSRC
CLNACC RCV000188393.1,