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rs879255276

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879255276(-;-)
Make rs879255276(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position40688411
GeneMAFB
is asnp
is mentioned by
dbSNPrs879255276
ebirs879255276
HLIrs879255276
Exacrs879255276
Varsomers879255276
Maprs879255276
PheGenIrs879255276
hapmaprs879255276
1000 genomesrs879255276
hgdprs879255276
ensemblrs879255276
gopubmedrs879255276
geneviewrs879255276
scholarrs879255276
googlers879255276
pharmgkbrs879255276
gwascentralrs879255276
openSNPrs879255276
23andMers879255276
23andMe allrs879255276
SNP Nexus

SNPshotrs879255276
SNPdbers879255276
MSV3drs879255276
GWAS Ctlgrs879255276
Max Magnitude0
ClinVar
Risk rs879255276(;)
Alt rs879255276(;)
Reference rs879255276(G;G)
Significance Pathogenic
Disease Duane syndrome type 3
Variation info
Gene MAFB
CLNDBN Duane syndrome type 3
Reversed 1
HGVS NC_000020.10:g.39317051delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000235078.1,