Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052807

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052807(A;A)
Make rs796052807(A;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100407902
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052807
ebirs796052807
HLIrs796052807
Exacrs796052807
Varsomers796052807
Maprs796052807
PheGenIrs796052807
hapmaprs796052807
1000 genomesrs796052807
hgdprs796052807
ensemblrs796052807
gopubmedrs796052807
geneviewrs796052807
scholarrs796052807
googlers796052807
pharmgkbrs796052807
gwascentralrs796052807
openSNPrs796052807
23andMers796052807
23andMe allrs796052807
SNP Nexus

SNPshotrs796052807
SNPdbers796052807
MSV3drs796052807
GWAS Ctlgrs796052807
Max Magnitude0
ClinVar
Risk rs796052807(A;A)
Alt rs796052807(A;A)
Reference rs796052807(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662900A>T
CLNSRC
CLNACC RCV000188358.2,