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rs796052795

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052795(C;C)
Make rs796052795(C;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100408237
GenePCDH19
is asnp
is mentioned by
dbSNPrs796052795
ebirs796052795
HLIrs796052795
Exacrs796052795
Varsomers796052795
Maprs796052795
PheGenIrs796052795
hapmaprs796052795
1000 genomesrs796052795
hgdprs796052795
ensemblrs796052795
gopubmedrs796052795
geneviewrs796052795
scholarrs796052795
googlers796052795
pharmgkbrs796052795
gwascentralrs796052795
openSNPrs796052795
23andMers796052795
23andMe allrs796052795
SNP Nexus

SNPshotrs796052795
SNPdbers796052795
MSV3drs796052795
GWAS Ctlgrs796052795
Max Magnitude0
ClinVar
Risk rs796052795(C;C)
Alt rs796052795(C;C)
Reference rs796052795(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663235C>G
CLNSRC
CLNACC RCV000188345.1,