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rs878853055

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853055(C;T)
Make rs878853055(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position80689977
GeneBRWD3
is asnp
is mentioned by
dbSNPrs878853055
ebirs878853055
HLIrs878853055
Exacrs878853055
Varsomers878853055
Maprs878853055
PheGenIrs878853055
hapmaprs878853055
1000 genomesrs878853055
hgdprs878853055
ensemblrs878853055
gopubmedrs878853055
geneviewrs878853055
scholarrs878853055
googlers878853055
pharmgkbrs878853055
gwascentralrs878853055
openSNPrs878853055
23andMers878853055
23andMe allrs878853055
SNP Nexus

SNPshotrs878853055
SNPdbers878853055
MSV3drs878853055
GWAS Ctlgrs878853055
Max Magnitude0
ClinVar
Risk rs878853055(T;T)
Alt rs878853055(T;T)
Reference rs878853055(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRWD3
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.79945476G>A
CLNSRC
CLNACC RCV000224684.1,