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rs398123603

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123603(A;G)
Make rs398123603(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position100408224
GenePCDH19
is asnp
is mentioned by
dbSNPrs398123603
ebirs398123603
HLIrs398123603
Exacrs398123603
Varsomers398123603
Maprs398123603
PheGenIrs398123603
hapmaprs398123603
1000 genomesrs398123603
hgdprs398123603
ensemblrs398123603
gopubmedrs398123603
geneviewrs398123603
scholarrs398123603
googlers398123603
pharmgkbrs398123603
gwascentralrs398123603
openSNPrs398123603
23andMers398123603
23andMe allrs398123603
SNP Nexus

SNPshotrs398123603
SNPdbers398123603
MSV3drs398123603
GWAS Ctlgrs398123603
Max Magnitude0
ClinVar
Risk rs398123603(G;G)
Alt rs398123603(G;G)
Reference rs398123603(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99663222T>C
CLNSRC
CLNACC RCV000079608.4,