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rs876661288

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661288(A;A)
Make rs876661288(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position9808900
GeneSBF2, SBF2-AS1
is asnp
is mentioned by
dbSNPrs876661288
ebirs876661288
HLIrs876661288
Exacrs876661288
Varsomers876661288
Maprs876661288
PheGenIrs876661288
hapmaprs876661288
1000 genomesrs876661288
hgdprs876661288
ensemblrs876661288
gopubmedrs876661288
geneviewrs876661288
scholarrs876661288
googlers876661288
pharmgkbrs876661288
gwascentralrs876661288
openSNPrs876661288
23andMers876661288
23andMe allrs876661288
SNP Nexus

SNPshotrs876661288
SNPdbers876661288
MSV3drs876661288
GWAS Ctlgrs876661288
Max Magnitude0
ClinVar
Risk rs876661288(A;A)
Alt rs876661288(A;A)
Reference rs876661288(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SBF2 SBF2-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.9830447C>T
CLNSRC
CLNACC RCV000217023.1,