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rs1064797376

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position100406878
GenePCDH19
is asnp
is mentioned by
dbSNPrs1064797376
dbSNP (old)rs1064797376
ClinGenrs1064797376
ebirs1064797376
HLIrs1064797376
Exacrs1064797376
Gnomadrs1064797376
Varsomers1064797376
Maprs1064797376
PheGenIrs1064797376
Biobankrs1064797376
1000 genomesrs1064797376
hgdprs1064797376
ensemblrs1064797376
gopubmedrs1064797376
geneviewrs1064797376
scholarrs1064797376
googlers1064797376
pharmgkbrs1064797376
gwascentralrs1064797376
openSNPrs1064797376
23andMers1064797376
23andMe allrs1064797376
SNPshotrs1064797376
SNPdbers1064797376
MSV3drs1064797376
GWAS Ctlgrs1064797376
Max Magnitude0
ClinVar
Risk rs1064797376(T;T)
Alt rs1064797376(T;T)
Reference Rs1064797376(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99661876C>A
CLNSRC
CLNACC RCV000488205.1,