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rs796052828

From SNPedia

Orientationminus
Make rs796052828(-;-)
Make rs796052828(-;TGAG)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100407536
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052828
ClinGenrs796052828
ebirs796052828
HLIrs796052828
Exacrs796052828
Varsomers796052828
Maprs796052828
PheGenIrs796052828
hapmaprs796052828
1000 genomesrs796052828
hgdprs796052828
ensemblrs796052828
gopubmedrs796052828
geneviewrs796052828
scholarrs796052828
googlers796052828
pharmgkbrs796052828
gwascentralrs796052828
openSNPrs796052828
23andMers796052828
23andMe allrs796052828
SNP Nexus

SNPshotrs796052828
SNPdbers796052828
MSV3drs796052828
GWAS Ctlgrs796052828
Max Magnitude
ClinVar
Risk
Alt
Reference Rs796052828(TGAG;TGAG)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662534_99662537delCTCA
CLNSRC
CLNACC RCV000188388.1,