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

rs796052844

From SNPedia

Orientationminus
Make rs796052844(-;-)
Make rs796052844(-;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100402756
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052844
ebirs796052844
HLIrs796052844
Exacrs796052844
Varsomers796052844
Maprs796052844
PheGenIrs796052844
hapmaprs796052844
1000 genomesrs796052844
hgdprs796052844
ensemblrs796052844
gopubmedrs796052844
geneviewrs796052844
scholarrs796052844
googlers796052844
pharmgkbrs796052844
gwascentralrs796052844
openSNPrs796052844
23andMers796052844
23andMe allrs796052844
SNP Nexus

SNPshotrs796052844
SNPdbers796052844
MSV3drs796052844
GWAS Ctlgrs796052844
Max Magnitude
ClinVar
Risk rs796052844(;)
Alt rs796052844(;)
Reference rs796052844(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99657754delT
CLNSRC
CLNACC RCV000188407.1,