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rs137853272

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137853272(A;G)
Make rs137853272(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position80677232
GeneBRWD3
is asnp
is mentioned by
dbSNPrs137853272
ebirs137853272
HLIrs137853272
Exacrs137853272
Varsomers137853272
Maprs137853272
PheGenIrs137853272
hapmaprs137853272
1000 genomesrs137853272
hgdprs137853272
ensemblrs137853272
gopubmedrs137853272
geneviewrs137853272
scholarrs137853272
googlers137853272
pharmgkbrs137853272
gwascentralrs137853272
openSNPrs137853272
23andMers137853272
23andMe allrs137853272
SNP Nexus

SNPshotrs137853272
SNPdbers137853272
MSV3drs137853272
GWAS Ctlgrs137853272
Max Magnitude0
OMIM300553
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137853272(G;G)
Alt rs137853272(G;G)
Reference rs137853272(A;A)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene BRWD3
CLNDBN Mental retardation, X-linked 93
Reversed 1
HGVS NC_000023.10:g.79932731T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011551.7,