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rs796052820

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052820(C;T)
Make rs796052820(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100406743
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052820
ebirs796052820
HLIrs796052820
Exacrs796052820
Varsomers796052820
Maprs796052820
PheGenIrs796052820
hapmaprs796052820
1000 genomesrs796052820
hgdprs796052820
ensemblrs796052820
gopubmedrs796052820
geneviewrs796052820
scholarrs796052820
googlers796052820
pharmgkbrs796052820
gwascentralrs796052820
openSNPrs796052820
23andMers796052820
23andMe allrs796052820
SNP Nexus

SNPshotrs796052820
SNPdbers796052820
MSV3drs796052820
GWAS Ctlgrs796052820
Max Magnitude0
ClinVar
Risk rs796052820(T;T)
Alt rs796052820(T;T)
Reference rs796052820(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99661741G>A
CLNSRC
CLNACC RCV000188375.1,