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

rs869312963

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312963(C;C)
Make rs869312963(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position9816961
GeneSBF2
is asnp
is mentioned by
dbSNPrs869312963
ebirs869312963
HLIrs869312963
Exacrs869312963
Varsomers869312963
Maprs869312963
PheGenIrs869312963
hapmaprs869312963
1000 genomesrs869312963
hgdprs869312963
ensemblrs869312963
gopubmedrs869312963
geneviewrs869312963
scholarrs869312963
googlers869312963
pharmgkbrs869312963
gwascentralrs869312963
openSNPrs869312963
23andMers869312963
23andMe allrs869312963
SNP Nexus

SNPshotrs869312963
SNPdbers869312963
MSV3drs869312963
GWAS Ctlgrs869312963
Max Magnitude0
ClinVar
Risk rs869312963(C;C)
Alt rs869312963(C;C)
Reference rs869312963(T;T)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene SBF2
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000011.9:g.9838508A>G
CLNSRC
CLNACC RCV000210630.1,