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rs796052802

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052802(C;T)
Make rs796052802(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100407979
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052802
ebirs796052802
HLIrs796052802
Exacrs796052802
Varsomers796052802
Maprs796052802
PheGenIrs796052802
hapmaprs796052802
1000 genomesrs796052802
hgdprs796052802
ensemblrs796052802
gopubmedrs796052802
geneviewrs796052802
scholarrs796052802
googlers796052802
pharmgkbrs796052802
gwascentralrs796052802
openSNPrs796052802
23andMers796052802
23andMe allrs796052802
SNP Nexus

SNPshotrs796052802
SNPdbers796052802
MSV3drs796052802
GWAS Ctlgrs796052802
Max Magnitude0
ClinVar
Risk rs796052802(T;T)
Alt rs796052802(T;T)
Reference rs796052802(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662977G>A
CLNSRC
CLNACC RCV000188352.1,