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rs869312970

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312970(A;G)
Make rs869312970(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position9832274
GeneSBF2
is asnp
is mentioned by
dbSNPrs869312970
ebirs869312970
HLIrs869312970
Exacrs869312970
Varsomers869312970
Maprs869312970
PheGenIrs869312970
hapmaprs869312970
1000 genomesrs869312970
hgdprs869312970
ensemblrs869312970
gopubmedrs869312970
geneviewrs869312970
scholarrs869312970
googlers869312970
pharmgkbrs869312970
gwascentralrs869312970
openSNPrs869312970
23andMers869312970
23andMe allrs869312970
SNP Nexus

SNPshotrs869312970
SNPdbers869312970
MSV3drs869312970
GWAS Ctlgrs869312970
Max Magnitude0
ClinVar
Risk rs869312970(G;G)
Alt rs869312970(G;G)
Reference rs869312970(A;A)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene SBF2
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000011.9:g.9853821T>C
CLNSRC
CLNACC RCV000210731.1,