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rs796052831

From SNPedia

Orientationminus
Make rs796052831(-;-)
Make rs796052831(-;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100407290
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052831
ebirs796052831
HLIrs796052831
Exacrs796052831
Varsomers796052831
Maprs796052831
PheGenIrs796052831
hapmaprs796052831
1000 genomesrs796052831
hgdprs796052831
ensemblrs796052831
gopubmedrs796052831
geneviewrs796052831
scholarrs796052831
googlers796052831
pharmgkbrs796052831
gwascentralrs796052831
openSNPrs796052831
23andMers796052831
23andMe allrs796052831
SNP Nexus

SNPshotrs796052831
SNPdbers796052831
MSV3drs796052831
GWAS Ctlgrs796052831
Max Magnitude
ClinVar
Risk rs796052831(;)
Alt rs796052831(;)
Reference rs796052831(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662288delG
CLNSRC
CLNACC RCV000188392.1,