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rs863224851

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224851(G;G)
Make rs863224851(G;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position80682607
GeneBRWD3
is asnp
is mentioned by
dbSNPrs863224851
ebirs863224851
HLIrs863224851
Exacrs863224851
Varsomers863224851
Maprs863224851
PheGenIrs863224851
hapmaprs863224851
1000 genomesrs863224851
hgdprs863224851
ensemblrs863224851
gopubmedrs863224851
geneviewrs863224851
scholarrs863224851
googlers863224851
pharmgkbrs863224851
gwascentralrs863224851
openSNPrs863224851
23andMers863224851
23andMe allrs863224851
SNP Nexus

SNPshotrs863224851
SNPdbers863224851
MSV3drs863224851
GWAS Ctlgrs863224851
Max Magnitude0
ClinVar
Risk rs863224851(G;G)
Alt rs863224851(G;G)
Reference rs863224851(T;T)
Significance Probable-Pathogenic
Disease Mental retardation
Variation info
Gene BRWD3
CLNDBN Mental retardation, X-linked 93
Reversed 1
HGVS NC_000023.10:g.79938106A>C
CLNSRC
CLNACC RCV000199586.1,