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

rs796052830

From SNPedia

Orientationminus
Make rs796052830(-;-)
Make rs796052830(-;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100407464
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052830
ebirs796052830
HLIrs796052830
Exacrs796052830
Varsomers796052830
Maprs796052830
PheGenIrs796052830
hapmaprs796052830
1000 genomesrs796052830
hgdprs796052830
ensemblrs796052830
gopubmedrs796052830
geneviewrs796052830
scholarrs796052830
googlers796052830
pharmgkbrs796052830
gwascentralrs796052830
openSNPrs796052830
23andMers796052830
23andMe allrs796052830
SNP Nexus

SNPshotrs796052830
SNPdbers796052830
MSV3drs796052830
GWAS Ctlgrs796052830
Max Magnitude
ClinVar
Risk rs796052830(;)
Alt rs796052830(;)
Reference rs796052830(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662462delT
CLNSRC
CLNACC RCV000188391.1,