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rs756414485

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs756414485(A;A)
Make rs756414485(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position100350665
GenePCDH19
is asnp
is mentioned by
dbSNPrs756414485
ebirs756414485
HLIrs756414485
Exacrs756414485
Varsomers756414485
Maprs756414485
PheGenIrs756414485
hapmaprs756414485
1000 genomesrs756414485
hgdprs756414485
ensemblrs756414485
gopubmedrs756414485
geneviewrs756414485
scholarrs756414485
googlers756414485
pharmgkbrs756414485
gwascentralrs756414485
openSNPrs756414485
23andMers756414485
23andMe allrs756414485
SNP Nexus

SNPshotrs756414485
SNPdbers756414485
MSV3drs756414485
GWAS Ctlgrs756414485
Max Magnitude0
ClinVar
Risk rs756414485(A,C;A,C)
Alt rs756414485(A,C;A,C)
Reference rs756414485(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH19
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.99605663G>A
CLNSRC
CLNACC RCV000188378.2,