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

rs796052800

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052800(A;A)
Make rs796052800(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100408135
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052800
ebirs796052800
HLIrs796052800
Exacrs796052800
Varsomers796052800
Maprs796052800
PheGenIrs796052800
hapmaprs796052800
1000 genomesrs796052800
hgdprs796052800
ensemblrs796052800
gopubmedrs796052800
geneviewrs796052800
scholarrs796052800
googlers796052800
pharmgkbrs796052800
gwascentralrs796052800
openSNPrs796052800
23andMers796052800
23andMe allrs796052800
SNP Nexus

SNPshotrs796052800
SNPdbers796052800
MSV3drs796052800
GWAS Ctlgrs796052800
Max Magnitude0
ClinVar
Risk rs796052800(A;A)
Alt rs796052800(A;A)
Reference rs796052800(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663133C>T
CLNSRC
CLNACC RCV000188350.1,