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rs1801239

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common on affy axiom data
(T;T) 0
Make rs1801239(A;G)
Make rs1801239(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position16877053
GeneCUBN
is asnp
is mentioned by
dbSNPrs1801239
dbSNP (classic)rs1801239
ClinGenrs1801239
ebirs1801239
HLIrs1801239
Exacrs1801239
Gnomadrs1801239
Varsomers1801239
LitVarrs1801239
Maprs1801239
PheGenIrs1801239
Biobankrs1801239
1000 genomesrs1801239
hgdprs1801239
ensemblrs1801239
geneviewrs1801239
scholarrs1801239
googlers1801239
pharmgkbrs1801239
gwascentralrs1801239
openSNPrs1801239
23andMers1801239
SNPshotrs1801239
SNPdbers1801239
MSV3drs1801239
GWAS Ctlgrs1801239
GMAF0.0528
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 21355061OA-icon.png]
Trait
Title CUBN Is a Gene Locus for Albuminuria
Risk Allele T
P-val 1E-11
Odds Ratio 0.0835 [NR] unit decrease (CKDGen)


[PMID 22574174OA-icon.png] CUBN as a Novel Locus for End-Stage Renal Disease: Insights from Renal Transplantation


[PMID 27197912OA-icon.png] Association Analysis of the Cubilin (CUBN) and Megalin (LRP2) Genes with ESRD in African Americans.


ClinVar
Risk rs1801239(G;G)
Alt rs1801239(G;G)
Reference Rs1801239(A;A)
Significance Probable-non-pathogenic
Disease Megaloblastic anemia
Variation info
Gene CUBN
CLNDBN Megaloblastic anemia
Reversed 1
HGVS NC_000010.10:g.16919052T>C
CLNSRC
CLNACC RCV000389104.1,



[PMID 30557881] Cubilin Single Nucleotide Polymorphism Variants are Associated with Macroangiopathy While a Matrix Metalloproteinase-9 Single Nucleotide Polymorphism Flip-Flop may Indicate Susceptibility of Diabetic Nephropathy in Type-2 Diabetic Patients.