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

rs796052796

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052796(A;A)
Make rs796052796(A;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100408229
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052796
ebirs796052796
HLIrs796052796
Exacrs796052796
Varsomers796052796
Maprs796052796
PheGenIrs796052796
hapmaprs796052796
1000 genomesrs796052796
hgdprs796052796
ensemblrs796052796
gopubmedrs796052796
geneviewrs796052796
scholarrs796052796
googlers796052796
pharmgkbrs796052796
gwascentralrs796052796
openSNPrs796052796
23andMers796052796
23andMe allrs796052796
SNP Nexus

SNPshotrs796052796
SNPdbers796052796
MSV3drs796052796
GWAS Ctlgrs796052796
Max Magnitude0
ClinVar
Risk rs796052796(A;A)
Alt rs796052796(A;A)
Reference rs796052796(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663227G>T
CLNSRC
CLNACC RCV000188346.1,