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rs1057518650

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518650(C;T)
Make rs1057518650(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position80745592
GeneBRWD3
is asnp
is mentioned by
dbSNPrs1057518650
dbSNP (old)rs1057518650
ClinGenrs1057518650
ebirs1057518650
HLIrs1057518650
Exacrs1057518650
Gnomadrs1057518650
Varsomers1057518650
LitVarrs1057518650
Maprs1057518650
PheGenIrs1057518650
Biobankrs1057518650
1000 genomesrs1057518650
hgdprs1057518650
ensemblrs1057518650
gopubmedrs1057518650
geneviewrs1057518650
scholarrs1057518650
googlers1057518650
pharmgkbrs1057518650
gwascentralrs1057518650
openSNPrs1057518650
23andMers1057518650
23andMe allrs1057518650
SNPshotrs1057518650
SNPdbers1057518650
MSV3drs1057518650
GWAS Ctlgrs1057518650
Max Magnitude0
ClinVar
Risk rs1057518650(T;T)
Alt rs1057518650(T;T)
Reference Rs1057518650(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene BRWD3
CLNDBN Mental retardation, X-linked 93
Reversed 1
HGVS NC_000023.10:g.80001091G>A
CLNSRC
CLNACC RCV000415462.1,