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rs1057524751

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524751(G;T)
Make rs1057524751(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position100407799
GenePCDH19
is asnp
is mentioned by
dbSNPrs1057524751
dbSNP (old)rs1057524751
ClinGenrs1057524751
ebirs1057524751
HLIrs1057524751
Exacrs1057524751
Gnomadrs1057524751
Varsomers1057524751
LitVarrs1057524751
Maprs1057524751
PheGenIrs1057524751
Biobankrs1057524751
1000 genomesrs1057524751
hgdprs1057524751
ensemblrs1057524751
gopubmedrs1057524751
geneviewrs1057524751
scholarrs1057524751
googlers1057524751
pharmgkbrs1057524751
gwascentralrs1057524751
openSNPrs1057524751
23andMers1057524751
23andMe allrs1057524751
SNPshotrs1057524751
SNPdbers1057524751
MSV3drs1057524751
GWAS Ctlgrs1057524751
Max Magnitude0
ClinVar
Risk rs1057524751(T;T)
Alt rs1057524751(T;T)
Reference Rs1057524751(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662797C>A
CLNSRC
CLNACC RCV000431864.1,