Have questions? Visit https://www.reddit.com/r/SNPedia

rs730882186

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730882186(-;-)
Make rs730882186(-;A)
Make rs730882186(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position80735165
GeneBRWD3
is asnp
is mentioned by
dbSNPrs730882186
ebirs730882186
HLIrs730882186
Exacrs730882186
Varsomers730882186
Maprs730882186
PheGenIrs730882186
hapmaprs730882186
1000 genomesrs730882186
hgdprs730882186
ensemblrs730882186
gopubmedrs730882186
geneviewrs730882186
scholarrs730882186
googlers730882186
pharmgkbrs730882186
gwascentralrs730882186
openSNPrs730882186
23andMers730882186
23andMe allrs730882186
SNP Nexus

SNPshotrs730882186
SNPdbers730882186
MSV3drs730882186
GWAS Ctlgrs730882186
Max Magnitude0
ClinVar
Risk rs730882186(A;A)
Alt rs730882186(A;A)
Reference rs730882186(;)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene BRWD3
CLNDBN Mental retardation, X-linked 93
Reversed 1
HGVS NC_000023.10:g.79990665dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000011550.7,