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

rs879253988

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879253988(C;T)
Make rs879253988(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome11
Position9808128
GeneSBF2, SBF2-AS1
is asnp
is mentioned by
dbSNPrs879253988
dbSNP (classic)rs879253988
ClinGenrs879253988
ebirs879253988
HLIrs879253988
Exacrs879253988
Gnomadrs879253988
Varsomers879253988
LitVarrs879253988
Maprs879253988
PheGenIrs879253988
Biobankrs879253988
1000 genomesrs879253988
hgdprs879253988
ensemblrs879253988
geneviewrs879253988
scholarrs879253988
googlers879253988
pharmgkbrs879253988
gwascentralrs879253988
openSNPrs879253988
23andMers879253988
SNPshotrs879253988
SNPdbers879253988
MSV3drs879253988
GWAS Ctlgrs879253988
Max Magnitude0
ClinVar
Risk rs879253988(T;T)
Alt rs879253988(T;T)
Reference Rs879253988(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SBF2 SBF2-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.9829675G>A
CLNSRC
CLNACC RCV000235454.1,