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

rs796052825

From SNPedia

Orientationminus
Make rs796052825(-;-)
Make rs796052825(-;ATC)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100408295
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052825
ebirs796052825
HLIrs796052825
Exacrs796052825
Varsomers796052825
Maprs796052825
PheGenIrs796052825
hapmaprs796052825
1000 genomesrs796052825
hgdprs796052825
ensemblrs796052825
gopubmedrs796052825
geneviewrs796052825
scholarrs796052825
googlers796052825
pharmgkbrs796052825
gwascentralrs796052825
openSNPrs796052825
23andMers796052825
23andMe allrs796052825
SNP Nexus

SNPshotrs796052825
SNPdbers796052825
MSV3drs796052825
GWAS Ctlgrs796052825
Max Magnitude
ClinVar
Risk rs796052825(;)
Alt rs796052825(;)
Reference rs796052825(ATC;ATC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663293_99663295delGAT
CLNSRC
CLNACC RCV000188385.1,