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rs796052837

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052837(C;G)
Make rs796052837(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100408100
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052837
ebirs796052837
HLIrs796052837
Exacrs796052837
Varsomers796052837
Maprs796052837
PheGenIrs796052837
hapmaprs796052837
1000 genomesrs796052837
hgdprs796052837
ensemblrs796052837
gopubmedrs796052837
geneviewrs796052837
scholarrs796052837
googlers796052837
pharmgkbrs796052837
gwascentralrs796052837
openSNPrs796052837
23andMers796052837
23andMe allrs796052837
SNP Nexus

SNPshotrs796052837
SNPdbers796052837
MSV3drs796052837
GWAS Ctlgrs796052837
Max Magnitude0
ClinVar
Risk rs796052837(G;G)
Alt rs796052837(G;G)
Reference rs796052837(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663098G>C
CLNSRC
CLNACC RCV000188398.1,