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

rs796052829

From SNPedia

Orientationminus
Make rs796052829(-;-)
Make rs796052829(-;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100407222
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052829
ebirs796052829
HLIrs796052829
Exacrs796052829
Varsomers796052829
Maprs796052829
PheGenIrs796052829
hapmaprs796052829
1000 genomesrs796052829
hgdprs796052829
ensemblrs796052829
gopubmedrs796052829
geneviewrs796052829
scholarrs796052829
googlers796052829
pharmgkbrs796052829
gwascentralrs796052829
openSNPrs796052829
23andMers796052829
23andMe allrs796052829
SNP Nexus

SNPshotrs796052829
SNPdbers796052829
MSV3drs796052829
GWAS Ctlgrs796052829
Max Magnitude
ClinVar
Risk rs796052829(;)
Alt rs796052829(;)
Reference rs796052829(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662220delT
CLNSRC
CLNACC RCV000188389.1,