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rs1057520761

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520761(A;A)
Make rs1057520761(A;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position100407773
GenePCDH19
is asnp
is mentioned by
dbSNPrs1057520761
dbSNP (old)rs1057520761
ClinGenrs1057520761
ebirs1057520761
HLIrs1057520761
Exacrs1057520761
Gnomadrs1057520761
Varsomers1057520761
Maprs1057520761
PheGenIrs1057520761
Biobankrs1057520761
1000 genomesrs1057520761
hgdprs1057520761
ensemblrs1057520761
gopubmedrs1057520761
geneviewrs1057520761
scholarrs1057520761
googlers1057520761
pharmgkbrs1057520761
gwascentralrs1057520761
openSNPrs1057520761
23andMers1057520761
23andMe allrs1057520761
SNPshotrs1057520761
SNPdbers1057520761
MSV3drs1057520761
GWAS Ctlgrs1057520761
Max Magnitude0
ClinVar
Risk rs1057520761(A;A)
Alt rs1057520761(A;A)
Reference Rs1057520761(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.99662771G>T
CLNSRC
CLNACC RCV000425887.1,